Identity
- Trade Name
- Rav Positioner Small FDA UDI
- Generic Name
- Inflatable extremity splint, reusable FDA UDI
- Device Name
- The function of the RAV Positioner is to provide adjustable wrist positioning, and to secure the wrist during arterial access procedures. The device is adjustable to accommodate the normal variation in hand sizes. It can be used on either the Right or Left wrist and is used for a limited period during the surgical procedure. The device is to be disposed of following the procedure. The RAV Wrist Positioners are non sterile and for single patient use only and are not intended to be cleaned and reused. FDA UDI
- Model / Reference
- 2030S FDA UDI
- Description
- The function of the RAV Positioner is to provide adjustable wrist positioning, and to secure the wrist during arterial access procedures. The device is adjustable to accommodate the normal variation in hand sizes. It can be used on either the Right or Left wrist and is used for a limited period during the surgical procedure. The device is to be disposed of following the procedure. The RAV Wrist Positioners are non sterile and for single patient use only and are not intended to be cleaned and reused. FDA UDI
Identifiers
- Catalog Number
- RAVP1000S FDA UDI
- Primary DI / UDI-DI
- 00856525007235 FDA UDI
- FDA Product Code
- FZF FDA UDI
- GMDN Term
- Inflatable extremity splint, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.3900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Inflatable extremity splint, reusable
Rav Positioner Small by Sun-Scientific Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Inflatable extremity splint, reusable.
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- First Aid Only — ACME UNITED CORP. · Class I
- DARCO® AirTraveler™ Walker Liner — DARCO International, Inc. · Class I
- DARCO® AirTraveler™ Walker Liner — DARCO International, Inc. · Class I
- DARCO® Night Splint — DARCO International, Inc. · Class I
- SC — Allied Medical LLC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Sun-Scientific Inc.
Sources (1)
- FDA UDI 5e221d2b-bbe8-4945-a27d-e03e2d3d4537 36 fields · synced May 29, 2026