Identity
- Trade Name
- LAZIC FDA UDI
- Generic Name
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable FDA UDI
- Device Name
- Bipolar forceps Non-Stick Micro-Series Bayonet 80° upwards Angeld, Tip 0,4 mm X 4 mm Working length 115 mm, Total length 230 mm, US-Pin FDA UDI
- Model / Reference
- 69.414.51 FDA UDI
- Description
- Bipolar forceps Non-Stick Micro-Series Bayonet 80° upwards Angeld, Tip 0,4 mm X 4 mm Working length 115 mm, Total length 230 mm, US-Pin FDA UDI
Identifiers
- Catalog Number
- 69.414.51 FDA UDI
- Primary DI / UDI-DI
- 04250603742432 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Open-surgery electrosurgical handpiece/electrode, bipolar, reusable 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
Lazic by Peter Lazic GmbH — 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
- Peter Lazic GmbH
Sources (1)
- FDA UDI 9ce91dd4-9b0c-467e-8a99-f79ee975fc35 35 fields · synced Jun 6, 2026