Identity
- Trade Name
- MicroFrance® FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
- Device Name
- MicroFrance® Curved scissors insert, blades 15 mm, tube CEV8649GP CEV649GP CEV9649GP and sheath CEV8649C5 CEV649C5 CEV9649C5 FDA UDI
- Model / Reference
- CEV605GP FDA UDI
- Description
- MicroFrance® Curved scissors insert, blades 15 mm, tube CEV8649GP CEV649GP CEV9649GP and sheath CEV8649C5 CEV649C5 CEV9649C5 FDA UDI
Identifiers
- Catalog Number
- CEV605GP FDA UDI
- Primary DI / UDI-DI
- 10381780094210 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MicroFrance® by Integra Microfrance — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Integra Microfrance
Sources (1)
- FDA UDI 8f146efb-2800-407f-9a43-5fa4383c6653 37 fields · synced May 31, 2026