Identity
- Trade Name
- KIT ARMPAD FULL W/2 SCREWS CLR FDA UDI
- Generic Name
- Wheelchair armrest FDA UDI
- Device Name
- Arm Pad w/ screws, Full-Length (13") FDA UDI
- Model / Reference
- 8881127509 FDA UDI
- Description
- Arm Pad w/ screws, Full-Length (13") FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841447114949 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wheelchair armrest
Kit Armpad Full W/2 Screws Clr by Invacare Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wheelchair armrest.
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- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- Hand Pad Horn Type — Otto Bock Mobility Solutions GmbH · Class I
- Kit for nut-modular armrest — Otto Bock Mobility Solutions GmbH · Class I
- 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
- Invacare Corp.
Sources (1)
- FDA UDI 2a8c39ae-7e65-4941-8158-8d390ace94d1 34 fields · synced May 31, 2026