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AMSCO Drying Cabinet

by Corporation Steris Canada 14 variants

AMSCO Drying Cabinet (DCR100101) is a Class II device made by Corporation Steris Canada, listed in FDA GUDID since 5 Feb 2021 (UDI-DI 00724995162610), 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 Number00724995162610 UDI-DI Date5 Feb 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  • Withdrawn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
Amsco
Generic name
Endoscope drying/storage cabinet
Model / Ref / Catalog
Drying Cabinet, DCR100101
Primary DI / UDI-DI
00724995162610
FDA product code
PUP
GMDN term
Endoscope drying/storage cabinet
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope drying/storage cabinet

Other devices from Corporation Steris Canada

See all devices from Corporation Steris Canada →

Properties

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