Identity
- Trade Name
- SQ.line® EUDAMEDSQ.LINE FDA UDI
- Generic Name
- Wire-extracting pliers FDA UDI
- Device Name
- Wire grasping forceps EUDAMEDSQ.LINE Wire Extraction Pliers, tapered, 6 1/4", (160 mm), double action, pointed, ergonomic handle, double articulated joint, non-sterile, reusable FDA UDI
- Model / Reference
- LX184NR EUDAMEDFDA UDI
- Description
- SQ.LINE Wire Extraction Pliers, tapered, 6 1/4", (160 mm), double action, pointed, ergonomic handle, double articulated joint, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- LX184NR FDA UDI
- Primary DI / UDI-DI
- 04046955285679 EUDAMEDFDA UDI
- Basic UDI-DI
- 403923900000033725 EUDAMED
- Direct Marketing DI
- 04046955285679 EUDAMED
- FDA Product Code
- HTC FDA UDI
- EMDN Code
- L091001 INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE EUDAMED
- GMDN Term
- Wire-extracting pliers FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 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
SQ.line® 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 | 403923900000033725 | 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 e218a028-d9b8-4822-b308-c511aa3fb07f 61 fields · synced Jul 25, 2026
- FDA UDI 17d435cf-247a-466d-ad7c-d7fdfb00fa24 35 fields · synced May 30, 2026