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Niagara MP21907

by Medisafe UK Limited

Niagara MP21907 (IW1055) is a Class II device made by Medisafe UK Limited, listed in FDA GUDID since 18 Mar 2021 (UDI-DI 05060247265247), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060247265247 UDI-DI Date18 Mar 2021ListedStatusListed 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  • Withdrawn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
Niagara
Generic name
Sterilizer/disinfector rack
Model / Ref / Catalog
MP21907, IW1055
Primary DI / UDI-DI
05060247265247
FDA product code
MEC
GMDN term
Sterilizer/disinfector rack
Device class
Class II
Regulation number
880.6992
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilizer/disinfector rack

Similar devices in this category

Other devices filed under Sterilizer/disinfector rack.

Other devices from Medisafe UK Limited

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Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)