Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
- Device Name
- ALPHATRIPART NEEDLE NOSE GRASP. FORCEPS ALPHATRIPART NEEDLE NOSE GRASP. FORCEPS Ø 5 MM, INSERT ONLY, DOUBLE ACTION FDA UDI
- Model / Reference
- Z.1436.30 FDA UDI
- Description
- ALPHATRIPART NEEDLE NOSE GRASP. FORCEPS ALPHATRIPART NEEDLE NOSE GRASP. FORCEPS Ø 5 MM, INSERT ONLY, DOUBLE ACTION FDA UDI
Identifiers
- Catalog Number
- Z.1436.30 FDA UDI
- Primary DI / UDI-DI
- 04049047112013 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
Gimmi by Gimmi GmbH — 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 |
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Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (1)
- FDA UDI 3b24a07c-fccf-4763-b6d9-d14c8844f31c 36 fields · synced May 31, 2026