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ProBP 2000 Digital Blood Pressure System

by Welch Allyn, Inc. 2 variants

Ref 2000-P, 2000 PLUS-CEModel 902123

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0732094GMN902123F6 Basic UDI-DI Date21 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Digital Blood Pressure System
Model / Reference
902123, 2000-P, 2000 PLUS-CE
Primary DI / UDI-DI
00732094252781, 00732094358612
Basic UDI-DI
0732094GMN902123F6
EMDN Code
Z1203020501, Z12040180
Device Class
Class IIa
Medical Purpose
Intended for use in measuring blood pressure and pulse rate.

Manufacturer details

EUDAMED SRN
US-PR-000047671

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Properties

Other properties (1)

  • Sterile: No