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Shaver blades JSBMV0001

by Joimax GmbH

Shaver blades JSBMV0001 is a Class I device made by Joimax GmbH, listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337104131), registry data as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250337104131 UDI-DI Date30 Dec 2022ListedStatusListed 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  • Withdrawn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
Shaver blades
Generic name
Arthroscopic shaver system, electrically-powered
Model / Ref / Catalog
JSBMV0001
Primary DI / UDI-DI
04250337104131
FDA product code
HWE
GMDN term
Arthroscopic shaver system, electrically-powered
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arthroscopic shaver system, electrically-powered

Similar devices

Other devices filed under FDA product code HWE (INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT).

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)