Identity
- Trade Name
- Nuvaderm FDA UDI
- Generic Name
- First aid absorbent pad/bandage FDA UDI
- Model / Reference
- Non-Sterile FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00866349000404 FDA UDI
- FDA Product Code
- KMF FDA UDI
- GMDN Term
- First aid absorbent pad/bandage FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5090 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid absorbent pad/bandage
Nuvaderm by Chesson Laboratory Associates, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as First aid absorbent pad/bandage.
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- H-Bandage Compression Dressing - Rolled — H & H Medical Corporation · Class I
- EMSRUN — Anji Hengfeng Sanitary Material Co., Ltd · Class I
- RHINO RESCUE — Wuxi Emsrun Technology Co., Ltd. · 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 |
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Manufacturer
- Manufacturer
- Chesson Laboratory Associates, Inc.
Sources (1)
- FDA UDI 71243bde-9a91-4661-bba6-8517f8f9ab93 32 fields · synced May 30, 2026