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Dissector H05-1006

by HOTRY (Beijing) Co., Ltd.

Dissector H05-1006 is a Class I device made by HOTRY (Beijing) Co., Ltd., listed in FDA GUDID since 27 Feb 2024 (UDI-DI 06975854250816), 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 Number06975854250816 UDI-DI Date27 Feb 2024ListedStatusListed 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  • Withdrawn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
Dissector
Generic name
Open-surgery dissector
Model / reference
H05-1006
Primary DI / UDI-DI
06975854250816
FDA product code
MDM
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery dissector

Other devices from HOTRY (Beijing) Co., Ltd.

See all devices from HOTRY (Beijing) Co., Ltd. →

Properties

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