PRP
PRP category pages help clinics organize supplies and supporting references.
Inventory is shipped from the US for domestic clinical fulfillment.
This hub covers platelet-rich plasma, an autologous (from the patient) blood concentrate.
Use this page to compare listed items and related clinical topics.
Inventory is listed for licensed clinics and credentialed healthcare teams.
PRP Workflow Overview
Most workflows start with whole-blood collection into sterile, labeled tubes. Teams then use centrifugation (spinning separation) to isolate a platelet-enriched layer. Final handling depends on the device system and the clinical protocol.
For orthopedic context and terminology, review Platelet Rich Plasma Advancements. Documentation often references device instructions for use and local standards. Maintain traceability from collection to final application.
- Confirm compatible tube size and rotor type before setup.
- Verify anticoagulant and material specifications per device labeling.
- Use aseptic technique for transfers and handling steps.
- Label intermediate containers to preserve patient traceability.
- Segregate clean and contaminated zones during processing.
- Record lot numbers for any single-use disposables used.
What You’ll Find in This Category
This category groups product listings used around PRP preparation and application workflows. Some practices use these items in orthopedics, dermatology, and aesthetic medicine. Content links provide context for related injection pathways and non-surgical options.
Items are sourced through vetted medical distributors for clinical supply channels.
- Listed preparation items, where available, with package-level details.
- Application adjuncts intended for professional procedure settings.
- Product pages with labeling and manufacturer information when provided.
- Related clinical reading to support staff training conversations.
- Navigation to compare other orthopedic injection categories and terms.
- Updates that reflect what is currently listed in this hub.
For a specific listing example, see Plasmolifting Gel 9 mL for pack configuration details. For joint injection comparisons that clinics may also stock, see Knee Pain Injection Options. For broader pathway discussions, review Non Surgical Alternatives.
How to Choose
Selection starts with defining the procedure setting and workflow constraints. PRP processing varies by device system, tube type, and handling steps. Match each listing to existing equipment and documented clinic protocols.
Consumables and Hardware Fit
- Tube volume and dimensions that fit available centrifuge buckets.
- Rotor type assumptions, including fixed-angle versus swing-bucket designs.
- Material and closure type that support safe handling and labeling.
- Sterility claims and packaging integrity indicators on arrival.
- Single-use versus multi-use components, based on labeling.
- Needle, transfer, or connector compatibility within the workflow.
- Waste stream considerations for blood-contacting disposables.
Quick tip: Keep a reference list of rotor model numbers and tube dimensions.
Workflow and Documentation Checks
- Manufacturer instructions for use and any included contraindication language.
- Lot tracking needs for audits and internal quality reviews.
- Clinic policy alignment for autologous blood handling steps.
- Staff training requirements for setup, labeling, and cleanup.
- Patient-consent workflow and charting templates used by the practice.
- Adjacent therapy planning, such as viscosupplement comparisons in OA.
When comparing knee injection pathways, reference Euflexxa Vs Orthovisc and Supartz Vs Euflexxa. For product-specific counseling frameworks, see Tailoring Hyalgan Plans. Keep comparisons descriptive and anchored to labeling and guidelines.
Safety and Use Notes
PRP workflows involve blood handling, device processing, and procedural applications. Safety planning should cover infection control, sharps management, and documentation rigor. Follow facility policies and the product labeling for each listed item.
Handling and Infection Control
- Treat all blood as potentially infectious during handling and cleanup.
- Use appropriate PPE and maintain a defined clean field.
- Confirm sterile barrier integrity before opening any packaged item.
- Dispose of sharps and blood-contact waste per facility policy.
- Avoid cross-contamination during transfers between containers and syringes.
- Do not use items with damaged packaging or unclear labeling.
- Document any incident per internal quality and safety procedures.
Why it matters: Traceability supports investigations when adverse events or defects are reported.
Evidence and Interpretation
Evidence quality varies by indication, technique, and outcome measure. Clinics should review specialty guidance and device labeling before protocol changes. For a neutral overview, see this AAOS resource: AAOS platelet-rich plasma overview.
For related joint-care context, review Cingal Injection Overview and Hymovis Injection Notes. For advanced OA discussions, see Synvisc Bone On Bone. Keep patient-specific decisions within local clinical governance.
Clinic Ordering and Compliance Notes
This PRP category supports wholesale supply workflows for professional settings. Ordering is restricted to licensed clinics and healthcare professionals. Maintain current credentials on file to avoid fulfillment delays.
- Create a clinic account and submit required licensing documentation.
- Use a verified business shipping address tied to the licensed entity.
- Review each listing for included components and packaging descriptions.
- Log lot numbers on receipt when the label provides them.
- Store items per labeled conditions and protect sterile packaging.
- Report damaged shipments per site return and claim procedures.
- Keep internal SOPs aligned with bloodborne pathogen requirements.
Listings prioritize authentic, brand-name products with manufacturer identification. Keep documentation aligned with internal audits and payer scrutiny. Product availability can change as inventory updates within this hub.
This content is for informational purposes only and is not a substitute for professional medical advice.
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Frequently Asked Questions
What does this PRP category include?
This category aggregates professional-use listings and related clinical context. It may include product pages used around platelet-rich plasma workflows. It also links to site posts that discuss orthopedic injection pathways. Use those links to compare terminology and clinical considerations. Product pages focus on packaging, labeling, and manufacturer details. This hub is designed for browsing and operational planning, not protocol selection.
How can a clinic confirm an item fits its centrifuge setup?
Start with the centrifuge model and rotor type in use. Confirm tube dimensions and maximum fill volume per the device IFU. Check whether adapters or balance tubes are required for safe runs. Review closure type and material compatibility with the rotor buckets. Document the selected configuration in an SOP for repeatability. If uncertainty remains, defer to the centrifuge manufacturer guidance and the tube labeling.
What documentation is typically required for wholesale access?
Wholesale access commonly requires proof of clinical licensure or facility credentials. Many suppliers also request a responsible clinician identifier and business contact details. A verified shipping address linked to the licensed entity is typical. Some accounts require periodic re-verification when licenses renew. Keep scanned documents current to reduce administrative delays. Requirements can vary by product category and local regulations.
What safety items should be considered for platelet-rich plasma handling workflows?
Workflows that include blood handling should align with facility bloodborne pathogen policies. PPE, sharps containers, and appropriate disinfectants support routine risk control. Use sterile supplies only when labeling specifies sterile status. Maintain clean and contaminated zones during processing steps. Track lot numbers when labels provide them for traceability. Report adverse events or product defects through internal quality systems and appropriate channels.
Where can clinicians review evidence and interpretation notes for PRP use?
Start with specialty society education pages and device labeling for the system in use. Orthopedic teams often consult AAOS resources for background discussions. Internal site posts can also help frame how clinics compare injection options. Examples include knee injection comparison pages and broader non-surgical pathway summaries. Use these sources to support staff education and documentation consistency. Final protocol decisions should follow local governance and supervising clinician judgment.
