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Susi®

EUDAMED

Class IIa (EU MDR)

Ref BV067SU

by Aesculap AG

Identity

Trade Name
SUSI® EUDAMED
Device Name
SUSI retractor EUDAMED
Model / Reference
BV067SU EUDAMED

Identifiers

Primary DI / UDI-DI
04046963186456 EUDAMED
Basic UDI-DI
4039239000000602ZW EUDAMED
EMDN Code
Z12019085 VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - CONSUMABLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Category: Surgical plume evacuation system tube

Susi® by Aesculap AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system tube.

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 e0386c4a-058c-4e99-8b70-f6f64739ee1c 61 fields · synced May 22, 2026