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Durogrip®

EUDAMED

Class I (EU MDR)

Ref BM183R

by Aesculap AG

Identity

Trade Name
DUROGRIP® EUDAMED
Device Name
Needle holder EUDAMED
Model / Reference
BM183R EUDAMED

Identifiers

Primary DI / UDI-DI
04038653028634 EUDAMED
Basic UDI-DI
403923900000038128 EUDAMED
Direct Marketing DI
04038653028634 EUDAMED
EMDN Code
L0205 NEEDLE HOLDERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

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

Durogrip® by Aesculap AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 0acf258e-e6bb-4660-a5c4-91e5cdc40cd1 61 fields · synced Jun 19, 2026