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Ebner Medical ER305.150E

by Ebner Medical LLC

Ebner Medical ER305.150E is a Class II device made by Ebner Medical LLC, listed in FDA GUDID since 10 Dec 2025 (UDI-DI 00840217910118), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840217910118 UDI-DI Date10 Dec 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  • Withdrawn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
Ebner Medical
Generic name
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
ER305.150E
Primary DI / UDI-DI
00840217910118
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

Similar devices

Other devices filed under FDA product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories).

Other devices from Ebner Medical LLC

See all devices from Ebner Medical LLC →

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)