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Ermis ER100.020BA

by Ermis MedTech GmbH

Ermis ER100.020BA is a Class II device made by Ermis MedTech GmbH, listed in FDA GUDID since 7 Oct 2025 (UDI-DI 04049224293504), 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 Number04049224293504 UDI-DI Date7 Oct 2025ListedStatusListed 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  • Withdrawn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
Ermis
Generic name
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
ER100.020BA
Primary DI / UDI-DI
04049224293504
FDA product code
KCT
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Ermis MedTech GmbH

See all devices from Ermis MedTech GmbH →

Properties

  • Sterilise before use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)