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Protab

EUDAMED

Class I (EU MDR)

Ref PT2634

by Bio Protech Inc.

Identity

Trade Name
PROTAB EUDAMED
Device Name
TAB Resting Electrodes EUDAMED
Model / Reference
PT2634 EUDAMED

Identifiers

Primary DI / UDI-DI
08809083943592 EUDAMED
Basic UDI-DI
880908394030KJ EUDAMED
EMDN Code
C020501 ECG ELECTRODES 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

Protab by Bio Protech Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Unknown

CE/MDR

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Manufacturer

Manufacturer
Bio Protech Inc.
EUDAMED SRN
KR-MF-000012687
Authorised Representative
Meridius Medical Europe Limited IE-AR-000004258

Sources (1)

  • EUDAMED 9d995cab-1ce5-4371-b8f1-80aa769e19cf 61 fields · synced May 23, 2026