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882061

by Steris Corporation

882061 is a Class II device made by Steris Corporation, listed in FDA GUDID since 17 Jan 2017 (UDI-DI 00724995003210), 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 Number00724995003210 UDI-DI Date17 Jan 2017ListedStatusListed 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  • Withdrawn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

Generic name
Sterilization packaging, single-use
Model / Ref / Catalog
882061
Primary DI / UDI-DI
00724995003210
FDA product code
FRG, KCT
GMDN term
Sterilization packaging, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Size
Length — 100 Feet
Width — 6 Inch

Related devices

Category: Sterilization packaging, single-use

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)