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SteriPod Sterilization Container CM-10011-851B

by Containmed, Inc.

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 Number00860010729281 UDI-DI Date29 Sep 2026ListedStatusListed 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  • Withdrawn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
SteriPod Sterilization Container
Generic Name
Sterilization container filter, single-use
Model / Ref / Catalog
CM-10011-851B
Primary DI / UDI-DI
00860010729281
FDA Product Code
KCT
GMDN Term
Sterilization container filter, single-use
Device Class
Class II
Regulation Number
880.6850
GUDID distribution status
In Commercial Distribution

Other devices from Containmed, Inc.

See all devices from Containmed, Inc. →

Properties

  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No