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HofHolder EHFS6342

by Joimax, Inc.

HofHolder EHFS6342 is a Class I device made by Joimax, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI 04250337121084), registry data as of 9 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250337121084 UDI-DI Date29 Oct 2026ListedStatusListed 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  • Withdrawn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
HofHolder
Generic name
Endoscope sheath, reusable
Model / reference
EHFS6342
Primary DI / UDI-DI
04250337121084
FDA product code
NBH
GMDN term
Endoscope sheath, reusable
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from Joimax, Inc.

See all devices from Joimax, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)