Identity
- Trade Name
- Drive FDA UDI
- Generic Name
- Attendant-only-propelled wheelchair, non-bariatric FDA UDI
- Device Name
- Sentra,26"HD.Det.FullArm,1/cs FDA UDI
- Model / Reference
- STD26DFA FDA UDI
- Description
- Sentra,26"HD.Det.FullArm,1/cs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00822383111551 FDA UDI
- FDA Product Code
- IOR FDA UDI
- GMDN Term
- Attendant-only-propelled wheelchair, non-bariatric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3850 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI cda4c9d4-40f1-4a37-ac01-e823728e8d20 34 fields · synced Jun 8, 2026