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Accu-PRO NIBP Cuff, Reusable, Single Tube, Bayonet, Infant

EUDAMED

Class I (EU MDR)

Ref APCR11010

by PROACT Medical Ltd.

Identity

Trade Name
Accu-PRO NIBP Cuff, Reusable, Single Tube, Bayonet, Infant EUDAMED
Device Name
Accu-PRO NIBP Cuff, Reusable EUDAMED
Model / Reference
APCR11010 EUDAMED

Identifiers

Primary DI / UDI-DI
25060179636553 EUDAMED
Basic UDI-DI
50560945APCRM7 EUDAMED
Unit of Use DI
15060179636556 EUDAMED
EMDN Code
Z12040180 GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Accu-PRO NIBP Cuff, Reusable, Single Tube, Bayonet, Infant by PROACT Medical Ltd. — 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

Manufacturer
PROACT Medical Ltd.
EUDAMED SRN
GB-MF-000006294
Authorised Representative
Acorn Regulatory Consultancy Services Ltd IE-AR-000000592

Sources (1)

  • EUDAMED 3bf2984a-b2a4-4894-90e7-4b0b427443ad 61 fields · synced Jul 9, 2026