Identity
- Trade Name
- SORBALGON 2X2 10/BX FDA UDI
- Generic Name
- Non-woven gauze pad FDA UDI
- Device Name
- SORBALGON 2X2 10/BX FDA UDI
- Model / Reference
- 49200000 FDA UDI
- Description
- SORBALGON 2X2 10/BX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10612553013641 FDA UDI
- FDA Product Code
- NAD FDA UDI
- GMDN Term
- Non-woven gauze pad FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4020 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Sorbalgon 2x2 10/Bx by Hartmann Usa Inc. — 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
- Hartmann Usa Inc.
Sources (1)
- FDA UDI 193ca99a-d701-4fdf-8daf-6c9902b8ae8d 34 fields · synced May 30, 2026