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Fleximeter®-Strips

EUDAMED

Class I (EU MDR)

Ref BK 253Model Fleximeter®-Strips

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
Fleximeter®-Strips EUDAMED
Model / Reference
Fleximeter®-Strips EUDAMED
BK 253 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK2531E EUDAMED
Basic UDI-DI
++E2108x0xFleximeterR5 EUDAMED
Unit of Use DI
+E210BK2530D EUDAMED
EMDN Code
Q010299 PROSTHETIC DENTISTRY DEVICES - OTHER 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

Fleximeter®-Strips by Dr. Jean Bausch 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-000005577

Sources (1)

  • EUDAMED afc9be2c-1615-40fc-90af-c8ee41d05e4d 61 fields · synced Jun 18, 2026