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Medline MPH1545BT

by Medline Industries, Inc.

Medline MPH1545BT is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 22 Nov 2023 (UDI-DI 00197344007595), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00197344007595 UDI-DI Date22 Nov 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Medline
Generic name
Glucose monitoring system IVD, home-use
Model / Ref / Catalog
MPH1545BT
Primary DI / UDI-DI
00197344007595
FDA product code
NBW
GMDN term
Glucose monitoring system IVD, home-use
Device class
Class II
Regulation number
862.1345
GUDID distribution status
In Commercial Distribution

Other devices from Medline Industries, Inc.

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Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)