Identity
- Trade Name
- Drive FDA UDI
- Generic Name
- Cubicle curtain, reusable FDA UDI
- Device Name
- Personal CareAids to Daily Living Product Description: Overdoor Exerc.Pulley,1/bx, RTL FDA UDI
- Model / Reference
- 13005 FDA UDI
- Description
- Personal CareAids to Daily Living Product Description: Overdoor Exerc.Pulley,1/bx, RTL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00822383102993 FDA UDI
- FDA Product Code
- ION FDA UDI
- GMDN Term
- Cubicle curtain, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5370 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: Cubicle curtain, reusable
Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cubicle curtain, reusable.
- DRIVEMEDICAL — Drive Devilbiss Healthcare · Class I
- DRIVEMEDICAL — Drive Devilbiss Healthcare · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI 8a3bb413-0e7b-4936-bc78-70a9763dcf54 33 fields · synced Jun 8, 2026