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Acculan 4

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref GP518R

by Aesculap AG

Identity

Trade Name
ACCULAN 4 EUDAMED
ELAN 4 FDA UDI
Generic Name
Surgical saw blade, oscillating, reusable FDA UDI
Device Name
ELAN 4/Acculan saw blade (RU) EUDAMED
SAW BLADE L SAGITTAL 35/10/0.5 FDA UDI
Model / Reference
GP518R EUDAMEDFDA UDI
Description
SAW BLADE L SAGITTAL 35/10/0.5 FDA UDI

Identifiers

Catalog Number
GP518R FDA UDI
Primary DI / UDI-DI
04046964775611 EUDAMEDFDA UDI
Basic UDI-DI
40392390000014612E EUDAMED
FDA Product Code
HBE FDA UDI
EMDN Code
Z12100980 INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Surgical saw blade, oscillating, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.4310 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

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

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED 20bb4e4f-42c4-40ef-b64f-00fd9fa77085 61 fields · synced Jun 18, 2026
  • FDA UDI 6937c586-0ad6-4f8b-b471-75a60f3fac48 36 fields · synced May 30, 2026