Identity
- Trade Name
- DUROGRIP® EUDAMEDAESCULAP FDA UDI
- Generic Name
- Orthopaedic implantable-device cutter FDA UDI
- Device Name
- Wire cutting forceps EUDAMEDTC Wire Cutting Forceps, 8 3/4", (220 mm), special hardened cutting edges, hard wire up to Ø 2.0 mm, soft wire up to Ø 3.0 mm, non-sterile, reusable FDA UDI
- Model / Reference
- LX152R EUDAMEDFDA UDI
- Description
- TC Wire Cutting Forceps, 8 3/4", (220 mm), special hardened cutting edges, hard wire up to Ø 2.0 mm, soft wire up to Ø 3.0 mm, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- LX152R FDA UDI
- Primary DI / UDI-DI
- 04038653049998 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000033827 EUDAMED
- Direct Marketing DI
- 04038653049998 EUDAMED
- FDA Product Code
- HXZ FDA UDI
- EMDN Code
- L01041202 WIRES AND METAL PLATES SCISSORS, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic implantable-device cutter 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Durogrip® by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 403923900000033827 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED d4c765b0-c898-4667-bddc-ea5e2efe2b5f 61 fields · synced Jul 9, 2026
- FDA UDI 704c59f8-f7e0-4370-b1c0-ec20b43ad7ee 35 fields · synced May 30, 2026