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Susi®

EUDAMED

Class IIa (EU MDR)

Ref BF047SU

by Aesculap AG

Identity

Trade Name
SUSI® EUDAMED
Device Name
SUSI forceps EUDAMED
Model / Reference
BF047SU EUDAMED

Identifiers

Primary DI / UDI-DI
04046963117757 EUDAMED
Basic UDI-DI
4039239000000600ZS 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 91aa354b-9ba8-47d8-87b7-d2fd33d2a25a 61 fields · synced May 22, 2026