Identity
- Trade Name
- Kroger FDA UDI
- Generic Name
- Non-woven gauze roll/sheet FDA UDI
- Device Name
- Rolled Gauze, 2 IN x 2.5 YDS FDA UDI
- Model / Reference
- 011110351241 FDA UDI
- Description
- Rolled Gauze, 2 IN x 2.5 YDS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00011110351241 FDA UDI
- FDA Product Code
- NAB FDA UDI
- GMDN Term
- Non-woven gauze roll/sheet FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Kroger by Kroger Co., The — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Kroger Co., The
Sources (1)
- FDA UDI 348fc6ac-258a-45a3-a34b-82a16c8376df 34 fields · synced Jun 1, 2026