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basti

EUDAMED

Class I (EU MDR)

Ref 56 01 000Ref 56 02 000Ref 56 04 000

by Schuchmann GmbH & Co. KG

Identity

Trade Name
basti EUDAMED
Device Name
Basti EUDAMED
Model / Reference
56 01 000 EUDAMED
56 02 000 EUDAMED
56 04 000 EUDAMED

Identifiers

Primary DI / UDI-DI
04251040203005 EUDAMED
04251040203012 EUDAMED
04251040203036 EUDAMED
Basic UDI-DI
4251040200004000560XXXXBV EUDAMED
Direct Marketing DI
04251040203005 EUDAMED
04251040203012 EUDAMED
04251040203036 EUDAMED
EMDN Code
Y093303,Y093312 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

basti by Schuchmann GmbH & Co. KG — 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

EUDAMED SRN
DE-MF-000013435

Sources (3)

  • EUDAMED 8818bdf3-c509-4ccf-b930-edf09f945563 61 fields · synced Jul 29, 2026
  • EUDAMED 6240c5a5-c170-4d7c-9d5e-f8bde790320b 61 fields · synced May 18, 2026
  • EUDAMED 2bbaabbf-aa72-4720-a9fd-7c49eb60d602 61 fields · synced May 18, 2026