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Viterion 100 TeleHealth Monitor 3.5.0.en

by Viterion Corporation

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852579007009 UDI-DI Date17 Oct 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Viterion 100 TeleHealth Monitor
Generic Name
Home healthcare information system
Model / Ref / Catalog
3.5.0.en, 81842478
Primary DI / UDI-DI
00852579007009
FDA Product Code
MWI
GMDN Term
Home healthcare information system
Device Class
Class II
Regulation Number
870.2300
GUDID distribution status
Not in Commercial Distribution
Size
Weight — 3.800 Pound
Depth — 3.900 Inch
Width — 9.720 Inch
Height — 7.680 Inch

Properties

  • Prescription Use
  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No