Fragmented documentation
Measurements and visit records spread across workflows or teams.
AOR Medical Solutions
Strengthen every stage of your wound care program.
Connect advanced solutions, digital documentation, education and support with AOR Medical Solutions.
An operational discussion about your organization, team and workflows—not a patient clinical evaluation.
Where does your program need support?
Category decisions
Technical information to organize and review with qualified professionals.
Team preparation
Education needs across roles, shifts and care settings.
Coordinated implementation
Responsibilities, preparation and follow-up to define together.
Solution areas
What your organization can request
Bring AOR your supply, documentation and team-preparation needs. Request confirmation of options in these categories, available technical materials and a written proposal for solutions confirmed for your institution and territory.
Assessment & documentation
- Need
- Connect measurements and visit records across the team.
- What to evaluate
- Capture methods, record structure and team access.
- Request from AOR
- Request an AOR HealIQ presentation and documentation to assess fit with your team's workflow.
Wound bed preparation
- Need
- Organize the team's review of cleansing and preparation categories.
- What to evaluate
- Official instructions, handling requirements and institutional protocols.
- Request from AOR
- Request confirmation of cleansing and preparation options, available technical documents and a written proposal for confirmed solutions.
Moisture & exudate
- Need
- Make dressing-category review easier to organize.
- What to evaluate
- Material characteristics, handling and clinical-team selection criteria.
- Request from AOR
- Request a review of dressing categories, technical materials and supply options for your territory; define education in the proposal.
Protection & offloading
- Need
- Coordinate pressure-related education and protection resources.
- What to evaluate
- Staff responsibilities, fitting requirements and care-setting protocols.
- Request from AOR
- Request confirmation of protection and offloading options, fitting requirements and any staff preparation within the agreed scope.
Biological & synthetic materials
- Need
- Structure the review of matrix and advanced-material categories.
- What to evaluate
- Official documentation, storage, traceability and professional-use requirements.
- Request from AOR
- Request confirmation of advanced-material options and available official documents before considering a supply proposal.
Complementary technologies
- Need
- Prepare the organization to evaluate device-based categories.
- What to evaluate
- Infrastructure, consumables, operator training and supervised-use requirements.
- Request from AOR
- Request a technical review of device categories, territory availability and equipment, consumable and training scope for confirmed solutions.
Supply categories are requests for confirmation, not a stock list. Your clinical team selects appropriate products using official instructions and institutional policies.
Explore the complete category libraryBuilt around your care setting
Wound clinics
Category review, visit documentation and staff education for an outpatient program.
Discuss needs for wound clinicsHospitals
Coordinate departments, clinical protocols and implementation requirements.
Discuss needs for hospitalsHome health
Plan field documentation, team training and service coordination across visits.
Discuss needs for home healthLong-term care
Organize handoffs, pressure-related education and documentation across shifts.
Discuss needs for long-term careAOR HealIQ
One organized digital workflow
Measurement, visit records and follow-up
AOR HealIQ brings wound measurement and documentation into a structured workflow on its separate official platform. Visit records, tracking between visits and a shared team view help organize documentation review. Review configuration and fit on the official platform with AOR.
Explore AOR HealIQClinical information and availabilityYour request, a written proposal, a defined scope
AOR connects your organizational priorities with confirmed options and a practical proposal. Supply, delivery, training and service commitments are specified for the selected solution—not assumed.
- 01
Share requirements
Describe the categories you need, your care setting, territory and team. AOR reviews the request and identifies what needs confirmation.
- 02
Confirm options & documents
Request an availability review and the available official technical documents for confirmed options, including handling or preparation requirements where documented.
- 03
Receive a written proposal
Review the exact solutions or supplies, costs, territory, responsibilities and terms. Implementation, training, delivery coordination and service appear only when part of the agreed scope.
- 04
Coordinate delivery & follow-up
After terms are agreed, coordinate the defined delivery and team preparation. Use the service contacts and follow-up arrangements specified in your agreement.
The scope of services is defined by the solution, territory and agreement. Availability, costs and responsibilities are confirmed in writing.
Resources for your next decision
Wound category education
The full dressing, device and advanced-material library, with precautions.
Open libraryTechnical documentation
Request category documentation and confirm which technical materials are available for your review.
Request documentationEducation & implementation
Explore AOR's documented training and implementation process.
Explore trainingProduct library
Explore the wound care library
Explore functions, use contexts and precautions by product type. Images are illustrative renderings, not manufacturer product photographs.
Level 1
Core dressing and device categories
Assessment and wound bed preparation (3)
Wound cleansers and irrigation solutions
Solutions used to cleanse or irrigate the wound and surrounding skin before assessment and dressing application.
Use context
- Routine dressing change procedures
Selection follows the organization's cleansing protocol and the product's official instructions.
Debridement aids
Pads, gels and single-use tools used to support removal of non-viable tissue and debris from the wound bed.
Use context
- Performed only by clinicians authorized under local scope of practice
Method selection is a clinical decision; AOR publishes no technique guidance.
Assessment and documentation tools
Measurement guides, imaging aids and structured record formats that make wound assessment repeatable between clinicians and shifts.
Use context
- Baseline and follow-up assessment across sites
- Continuity of care and administrative review support
Consistency of method matters more than any single tool; training is included in AOR programs.
Moisture and exudate management (4)
Hydrocolloid dressings
Self-adhesive dressing that forms a gel as it interacts with wound fluid, maintaining a moist wound environment under an occlusive cover.
Use context
- Wounds with light to moderate drainage
- Situations where fewer dressing changes are preferred
Wear time, odour on removal and periwound skin tolerance are assessed by the clinical team.
Hydrogels
Water- or glycerin-based gel, sheet or impregnated gauze that adds moisture to a dry wound bed.
Use context
- Dry or minimally draining wounds
- Support for autolytic wound bed preparation
Usually needs a secondary dressing; excess moisture on surrounding skin is monitored.
Foam dressings
Absorbent polyurethane dressing that takes up wound fluid while cushioning the wound; available with or without adhesive borders.
Use context
- Moderate to heavy exudate
- Areas needing cushioning or pressure redistribution support
Thickness, border type and conformability differ across shapes and anatomical sites.
Alginate and gelling fibre dressings
Fibrous dressing that absorbs high volumes of fluid and converts to a gel, conforming to the shape of the wound including cavities.
Use context
- Heavily draining wounds
- Cavity or undermined wounds requiring packing
Requires a secondary cover dressing and complete removal at each change.
Protection, securement and offloading (6)
Gauze and non-adherent primary dressings
Basic contact layer placed directly on the wound to cover it and allow drainage to pass through to a secondary dressing.
Use context
- General wound coverage where a simple contact layer is used
- Combined with a secondary absorbent or securement layer
Frequency of change, adherence to the wound bed and comfort at removal vary by construction.
Transparent film dressings
Thin adhesive sheet that covers the wound, allows visual inspection without removal and acts as a barrier to outside contamination and water.
Use context
- Low-exudate wounds and intact skin protection
- Securing another dressing in place
Not absorbent on its own; skin condition around the wound guides adhesive selection.
Periwound skin protectants and barriers
Films, creams and barrier products applied to the skin around the wound to reduce exposure to moisture and adhesive stress.
Use context
- Wounds with heavy exudate or frequent dressing changes
Compatibility with the chosen dressing adhesive is confirmed before routine use.
Compression systems
Bandages, wraps and garments that apply graduated external pressure to the limb as part of a prescribed program.
Use context
- Applied only after the required vascular assessment defined by the organization
Application technique, pressure level and reassessment intervals are clinician-determined.
Offloading and pressure redistribution devices
Footwear, inserts, boots, cushions and surfaces that redirect pressure away from an at-risk or existing wound site.
Use context
- Prevention protocols in long-term care and acute settings
- Programs pairing devices with repositioning schedules
Fit, adherence and staff training determine whether the device performs as intended.
Securement: tapes, wraps and bandages
Retention products that hold a primary dressing in place without adding absorbency.
Use context
- Any dressing regimen that needs a separate retention layer
Adhesive type is matched to skin fragility to reduce medical adhesive-related skin injury risk.
Advanced modalities (3)
Antimicrobial dressings
Dressings that incorporate an antimicrobial agent within the dressing material as part of a wound bioburden management strategy.
Use context
- Used within protocols defined by the treating organization
Agent, duration of use and review intervals are governed by clinical policy and the manufacturer's instructions for use.
Collagen and matrix dressings
Scaffold-type dressings applied to the wound bed as part of an advanced wound bed preparation strategy.
Use context
- Selected by specialist wound teams within an existing care pathway
Product-specific handling, storage and application steps must follow the official instructions for use.
Negative pressure wound therapy (NPWT) systems
A pump, sealed dressing kit and canister that apply controlled sub-atmospheric pressure to a sealed wound and collect exudate.
Use context
- Managed by trained staff under a defined therapy order
- Institutional and, where supported, supervised home programs
Training, alarm response, seal integrity and consumable supply planning are part of deployment.
Biologic, synthetic and regenerative categories (12)
Advanced materials and technologies reviewed by the clinical team within its care protocols.
Skin substitutes (cellular and tissue-based products)
What it is
A family of sheet, disc or particulate products made from bioengineered, human or animal-derived tissue that is applied directly to a prepared wound bed.
What it does
Provides a temporary biological cover and structural scaffold over the wound bed, used within an advanced pathway after standard care and wound bed preparation.
Selection, application interval and total number of applications follow the treating organization's pathway and the manufacturer's official instructions for use.
Human allografts (donated human tissue)
What it is
Processed human skin or soft-tissue grafts recovered from donors through an accredited tissue bank and supplied cryopreserved, refrigerated or dehydrated.
What it does
Places donor-derived tissue over the wound as a biological cover and matrix during an advanced treatment phase.
Donor screening, chain of custody, storage temperature and expiry handling are governed by tissue-bank standards and institutional policy.
Xenografts and acellular dermal matrices
What it is
Animal-derived tissue (commonly porcine or bovine) processed to remove cellular components, leaving a structural extracellular matrix.
What it does
Supplies a matrix scaffold at the wound surface as part of advanced wound bed preparation strategies.
Patient sensitivity, cultural or dietary preferences and material sourcing are confirmed before use.
Amniotic membrane allografts
What it is
Thin membrane tissue recovered from donated placental tissue after consented, screened caesarean delivery, supplied dehydrated or cryopreserved.
What it does
Applied as a thin biological covering over a prepared wound bed within an advanced treatment protocol.
Rehydration steps, orientation of the membrane and securement method follow the manufacturer's official instructions.
Placental and umbilical cord tissue allografts
What it is
Tissue allografts derived from other components of the birth tissue complex, including chorion layers and umbilical cord tissue.
What it does
Used as a biological covering or matrix layer in advanced wound pathways, typically in sheet or disc format sized to the wound.
Storage conditions, thaw or rehydration handling and single-patient use requirements are defined by the supplier.
Collagen dressings and collagen matrices
What it is
Purified collagen, alone or combined with other materials such as oxidized regenerated cellulose or alginate, supplied as pads, particles, gels or sheets.
What it does
Adds a collagen-based scaffold material to the wound bed as part of a structured advanced wound bed preparation approach.
Format (pad, particle or gel), moisture level of the wound and the secondary dressing choice all influence handling.
Platelet-rich plasma (PRP) and autologous blood-derived preparations
What it is
Preparations produced at the point of care from the patient's own blood using a closed centrifugation system, delivered as a liquid, gel or fibrin matrix.
What it does
Applies an autologous preparation to the wound bed within a defined procedural protocol carried out by trained clinicians.
Blood draw, processing parameters, sterility, documentation and operator training are all governed by institutional procedure.
Growth factor products
What it is
Topical formulations that contain a defined growth factor component, supplied as gels or impregnated carriers.
What it does
Delivers the formulation to the wound surface under a prescribed application schedule and dressing regimen.
Prescribing rules, storage temperature, application frequency and treatment duration are set by the official labeling.
Acellular fish skin matrices
What it is
Intact, minimally processed marine-derived matrices supplied as dry sheets that are rehydrated before application.
What it does
Places a porous matrix over the wound bed as an advanced-pathway alternative to mammalian-derived matrices.
Fish allergy status is confirmed before use; rehydration and fenestration steps follow the official instructions.
Autologous epidermal grafting and cell harvesting systems
What it is
Devices that harvest small epidermal micrografts or a cell suspension from the patient's own donor site at the point of care.
What it does
Transfers autologous epidermal tissue or cells from a donor site to the prepared wound within a single documented procedure.
Donor-site selection and aftercare, procedure time and operator certification are part of program planning.
Hyaluronic acid based technologies
What it is
Gels, sheets and impregnated carriers built around hyaluronic acid or its esters.
What it does
Applies a hydrated matrix layer to the wound surface, typically covered by a secondary dressing.
Change frequency and compatibility with the secondary dressing are defined by the official instructions for use.
Topical oxygen therapy systems
What it is
Devices that deliver oxygen to a sealed wound chamber, wrap or dressing interface, in clinic-based or continuous-wear formats.
What it does
Maintains an oxygen-enriched environment at the dressing interface for the duration defined in the therapy order.
Seal integrity, consumable supply, device training and alarm response are part of deployment planning.
Clinical information and availability
This library explains generic product types for program planning. It is not a branded portfolio or a treatment recommendation. Selection and use remain with qualified professionals, organizational protocols and the manufacturer's official instructions.
AOR confirms available solutions, territory, service scope and terms for each engagement. Regulatory status must be verified for the specific product and jurisdiction; this page implies no approval or guarantee of efficacy, healing, coverage or reimbursement.
- Source URL
- AOR-authored category education
- Last verified
- 2026-08-02
- Content status
- Verified AOR category education
Discuss your needs. Define the next steps.
Share the categories, documentation or team preparation you need. AOR will review options for confirmation and the next step toward a written proposal.
Educational content only—not medical advice, a treatment protocol or regulatory clearance. Clinical decisions belong to qualified professionals. Follow organizational policies and manufacturer instructions for use.