Identity
- Trade Name
- ACCULAN 4 EUDAMEDELAN 4 FDA UDI
- Generic Name
- Surgical saw blade, sagittal, single-use FDA UDI
- Device Name
- ELAN 4/Acculan saw blade (SU) EUDAMEDDISP.SAW BLADE L SAGITTAL 20/15/6 FDA UDI
- Model / Reference
- GP526SU EUDAMEDFDA UDI
- Description
- DISP.SAW BLADE L SAGITTAL 20/15/6 FDA UDI
Identifiers
- Catalog Number
- GP526SU FDA UDI
- Primary DI / UDI-DI
- 04046955157358 EUDAMEDFDA UDI
- Basic UDI-DI
- 40392390000014622G EUDAMED
- FDA Product Code
- HBE FDA UDI
- EMDN Code
- Z12100980 INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Surgical saw blade, sagittal, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4310 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Acculan 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 | 40392390000014622G | 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 71b4e07c-6da2-4aed-ad67-8002057ee4ea 61 fields · synced Jul 9, 2026
- FDA UDI 5ea1f183-706d-4fac-8bc7-06ffd9f74d3d 35 fields · synced May 29, 2026