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URS. 031.06.4250a

EUDAMED

Class IIa (EU MDR)

Ref 9AMB-1012

by Blazejewski MEDI-TECH GmbH

Identity

Device Name
URS. 031.06.4250a EUDAMED
Model / Reference
9AMB-1012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-9AMB-1012FZ EUDAMED
Basic UDI-DI
B-9AMB-1012FZ EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Flexible video ureteroscope, single-use

URS. 031.06.4250a by Blazejewski MEDI-TECH GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video ureteroscope, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000005467

Sources (1)

  • EUDAMED a0364e68-dca9-483c-a9d3-3b49b3eb415b 61 fields · synced Jun 17, 2026