Identity
- Trade Name
- Avaline Medical NJ LLC FDA UDI
- Generic Name
- Non-woven gauze pad FDA UDI
- Device Name
- 3x4 Non-Adherent Pads 100x2 FDA UDI
- Model / Reference
- NAP3X4X200 FDA UDI
- Description
- 3x4 Non-Adherent Pads 100x2 FDA UDI
Identifiers
- Catalog Number
- NAP3X4X200 FDA UDI
- Primary DI / UDI-DI
- 00650415208913 FDA UDI
- FDA Product Code
- NAB FDA UDI
- GMDN Term
- Non-woven gauze pad 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
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Avaline Medical NJ LLC by Avaline Medical NJ Limited Liability Company — 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
- Avaline Medical NJ Limited Liability Company
Sources (1)
- FDA UDI 5a4f411e-3098-4b00-860f-7d219bc16ca2 36 fields · synced Jun 1, 2026