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MedLite ID IDA01-CR

by Medlite ID

Listed FDA GUDID listing, no authorization on record

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850011772003 UDI-DI Date20 Jan 2023ListedStatusListed GUDID: 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  • Withdrawn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
MedLite ID
Generic Name
Intravenous line identification light
Model / Reference
IDA01-CR
Primary DI / UDI-DI
00850011772003
FDA Product Code
QMX
GMDN Term
Intravenous line identification light
Device Class
Class I
Regulation Number
878.4800
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Intravenous line identification light

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

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