Identity
- Trade Name
- Smith and Nephew FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed FDA UDI
- Device Name
- Eliminator 90 w/Integrated Cable Wand, fits 5.5 mm cannula, 90 deg., not malleable FDA UDI
- Model / Reference
- AC1345-01 FDA UDI
- Description
- Eliminator 90 w/Integrated Cable Wand, fits 5.5 mm cannula, 90 deg., not malleable FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810041638489 FDA UDI
- FDA Product Code
- NUJ FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
Smith and Nephew by Provision — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Provision
Sources (1)
- FDA UDI 42cc2d0a-e993-4c15-b488-21eed7a5cd67 35 fields · synced May 30, 2026