Identity
- Trade Name
- Protekt Parts FDA UDI
- Generic Name
- Wheelchair armrest FDA UDI
- Device Name
- Adjustable-Height Arm Assembly f/ K3 - Full Arm Left (STDS3J24AFL) FDA UDI
- Model / Reference
- PP-AHFAASMK3LFT FDA UDI
- Description
- Adjustable-Height Arm Assembly f/ K3 - Full Arm Left (STDS3J24AFL) FDA UDI
Identifiers
- Catalog Number
- PP-AHFAASMK3LFT FDA UDI
- Primary DI / UDI-DI
- 05060488573316 FDA UDI
- FDA Product Code
- IML FDA UDI
- GMDN Term
- Wheelchair armrest FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3920 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Dimensions & Sizes
- Size
- Width — 2 Inch FDA UDIHeight — 4 Inch FDA UDILength — 8 Inch FDA UDI
Category: Wheelchair armrest
Protekt Parts by Proactive Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Wheelchair armrest.
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- Hand Pad Palm Extenser — Otto Bock Mobility Solutions GmbH · 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
- Proactive Medical Products
Sources (1)
- FDA UDI caddabf6-4173-4cdd-ae27-5f78ad9611f3 36 fields · synced Jun 1, 2026