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ViewFlex™ H701375

by St. Jude Medical, Inc.

Ref H701375

ViewFlex™ H701375 is a Class I device made by St. Jude Medical, Inc., registered in EUDAMED on 24 Aug 2026 (Basic UDI-DI 5414734DMC0013CC) and listed in FDA GUDID since 6 May 2016 (UDI-DI 05415067013750), active as of 25 Oct 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5414734DMC0013CC Basic UDI-DI 05415067013750UDI-DIDate24 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05415067013750 UDI-DI Date6 May 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 5414734DMC0013CC registered 24 Aug 2026 Active
  • FDA GUDID UDI-DI 05415067013750 listed 6 May 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05415067013750
  2. Registered EUDAMED 5414734DMC0013CC

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  • Withdrawn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
ViewFlex™
Generic name
Electrical-only medical device connection cable, reusable
Device name
ViewFlex Catheter Input Module
Model / Ref / Catalog
H701375
Primary DI / UDI-DI
05415067013750
Basic UDI-DI
5414734DMC0013CC
FDA product code
DRJ
EMDN code
Z11049080 Various ultrasound instruments - hardware accessories
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I
Regulation number
870.2600
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under VARIOUS ULTRASOUND INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from St. Jude Medical, Inc.

See all devices from St. Jude Medical, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)