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Sncdt-365

by Medyssey Co., Ltd.

Sncdt-365 is a Class I device made by Medyssey Co., Ltd., listed in FDA GUDID since 27 Jun 2023 (UDI-DI 08800048455259), 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 Number08800048455259 UDI-DI Date27 Jun 2023ListedStatusListed 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  • Withdrawn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

Generic name
Bone tap, reusable
Model / reference
SNCDT-365
Primary DI / UDI-DI
08800048455259
FDA product code
LXH
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

Other devices from Medyssey Co., Ltd.

See all devices from Medyssey Co., Ltd. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)