Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Non-woven gauze pad, non-sterile FDA UDI
- Device Name
- Post-Op Gauze Sponges 4 x 4in. (10.2 x 10.2cm) Nonwoven with Cellulose Center. Non Sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. FDA UDI
- Model / Reference
- C-NSG33 FDA UDI
- Description
- Post-Op Gauze Sponges 4 x 4in. (10.2 x 10.2cm) Nonwoven with Cellulose Center. Non Sterile. Single Use Only. Not Made with Natural Rubber Latex. Store in a Cool, Dry Place. FDA UDI
Identifiers
- Catalog Number
- C-NSG33 FDA UDI
- Primary DI / UDI-DI
- 20885380133722 FDA UDI
- FDA Product Code
- NAB FDA UDI
- GMDN Term
- Non-woven gauze pad, non-sterile FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4014 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Non-woven gauze pad, non-sterile
Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 45393685-c4d0-4217-9e00-53bb07b83f72 34 fields · synced Jun 8, 2026