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ivWatch Sensor Receptacle Model 400

by Ivwatch, LLC

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number00814088020016 UDI-DI Date14 Sep 2016ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number— Date—StatusActive

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  • Withdrawn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
ivWatch Sensor Receptacle
Generic Name
Intravenous access site monitoring system fibreoptic cable holder
Model / Reference
Model 400
Primary DI / UDI-DI
00814088020016
FDA Product Code
PMS
GMDN Term
Intravenous access site monitoring system fibreoptic cable holder
Device Class
Class II
Regulation Number
880.5725
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Depth — 0.42 Inch
Width — 1.31 Inch
Length — 2.25 Inch

Other devices from Ivwatch, LLC

See all devices from Ivwatch, LLC →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No