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Meritrans DTXPlus®

by Merit Medical Singapore Pte. Ltd. 57 variants

Ref 682021/AModel Meritrans DTXPlus®

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00884450322567 Basic UDI-DI 00884450322567UDI-DIDate20 Aug 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
DTX / DTX Kits
Model / Reference
Meritrans DTXPlus®, 682021/A
Primary DI / UDI-DI
00884450322567
Basic UDI-DI
B-00884450322567
EMDN Code
Z1203020301 Invasive blood pressure monitoring instruments
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
SG-MF-000002111
Authorised representative
Merit Medical Ireland Ltd IE-AR-000001011

Other devices from Merit Medical Singapore Pte., Ltd.

See all devices from Merit Medical Singapore Pte., Ltd. →

Properties

  • Sterile
  • Animal Tissues

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No