Identity
- Trade Name
- DRIVEMEDICAL FDA UDI
- Generic Name
- Bedrail FDA UDI
- Device Name
- BedsAccessories Product Description: HiDensityFoamTriFoldFloormat24x66x2,1/ea FDA UDI
- Model / Reference
- 7095-MED-TF FDA UDI
- Description
- BedsAccessories Product Description: HiDensityFoamTriFoldFloormat24x66x2,1/ea FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00822383522128 FDA UDI
- FDA Product Code
- IKY FDA UDI
- GMDN Term
- Bedrail FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5150 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bedrail
Drivemedical by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Medline — MEDLINE INDUSTRIES, INC. · Class II
- Composite Swing Rail — Dynarex Corp. · Class I
- Expansion Kit for D300 — Dynarex Corp. · Class I
- Ritter — Midmark Corporation · 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
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI d1b9fc9b-56f7-4cc7-96f8-09be85b3fe3d 33 fields · synced Jun 6, 2026