Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- ENT wire-cutting scissors FDA UDI
- Device Name
- Surgical Instrument EUDAMEDUNIVERSAL WIRE SCISSORS TC LENGTH 120 MM FDA UDI
- Model / Reference
- AA.1998.12 EUDAMEDFDA UDI
- Description
- UNIVERSAL WIRE SCISSORS TC LENGTH 120 MM FDA UDI
Identifiers
- Catalog Number
- AA.1998.12 FDA UDI
- Primary DI / UDI-DI
- 04049047006299 EUDAMEDFDA UDI
- Basic UDI-DI
- 4049047LCN03ANA27DRONF EUDAMED
- Direct Marketing DI
- 04049047006299 EUDAMED
- FDA Product Code
- HXZ FDA UDI
- EMDN Code
- L091002 INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
- GMDN Term
- ENT wire-cutting scissors FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
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
Category: ENT wire-cutting scissors
Gimmi by Gimmi GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as ENT wire-cutting scissors.
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- SCISSORS — KLS-Martin L.P. · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Trinity Sterile, Inc. — TRINITY STERILE, INC. · Class I
- Ambler Value Line — Ambler Surgical, LLC · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (2)
- FDA UDI f8415992-bb71-491c-a599-03e0131cd84c 34 fields · synced Jul 15, 2026
- EUDAMED 79b8324d-634e-4221-a021-bc6d2afb6e8b 61 fields · synced Jul 15, 2026