Identity
- Trade Name
- ELAN 4 EUDAMEDFDA UDI
- Generic Name
- Surgical instrument guard, reusable FDA UDI
- Device Name
- ELAN 4 MIS handpiece shaft EUDAMEDELAN 4 MIS HANDPIECE SHAFT L10 STRAIGHT FDA UDI
- Model / Reference
- GB920R EUDAMEDFDA UDI
- Description
- ELAN 4 MIS HANDPIECE SHAFT L10 STRAIGHT FDA UDI
Identifiers
- Catalog Number
- GB920R FDA UDI
- Primary DI / UDI-DI
- 04046964726170 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000014542H EUDAMED
- Direct Marketing DI
- 04046964726170 EUDAMED
- FDA Product Code
- HBB FDA UDI
- EMDN Code
- Z12100980 INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Surgical instrument guard, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4370 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
No
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Elan 4 by Aesculap AG — Class IIa — 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 | 40392390000014542H | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 718ae0bc-4320-4114-bed2-e21bba210979 61 fields · synced Jun 6, 2026
- FDA UDI b4811f28-3b72-499c-8c19-b8611e433243 35 fields · synced May 30, 2026