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Tempus Pro 2-Channel Invasive Pressure Universal Cable

by Remote Diagnostic Technologies Ltd.

Ref 01-2108 / 989706000681

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number506047244BM725VD Basic UDI-DI 05060472440716UDI-DIDate8 Jan 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number05060472440716 UDI-DI Date4 Oct 2016ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Tempus Pro 2-Channel Invasive Pressure Universal Cable EUDAMED
Tempus Pro GUDID
Generic Name
Multiple vital physiological parameter monitoring system, clinical
Device Name
Invasive Blood Pressure Cables
Model / Reference
01-2108 / 989706000681 EUDAMED
01-2108 GUDID
Primary DI / UDI-DI
05060472440716
Basic UDI-DI
506047244BM725VD
FDA Product Code
MHX
EMDN Code
Z1203020301 Invasive blood pressure monitoring instruments
GMDN Term
Multiple vital physiological parameter monitoring system, clinical
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
870.1025
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
01-2108 / 989706000681
GUDID
01-2108
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
GB-MF-000002127
Authorised representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

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Category: In-line arterial blood sampling set

Other devices from Remote Diagnostic Technologies Limited

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No