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InnoFine JSM-089

by JingFang Precision Medical Device(Shenzhen) Co., Ltd.

InnoFine JSM-089 is a Class II device made by JingFang Precision Medical Device(Shenzhen) Co., Ltd., listed in FDA GUDID since 21 Feb 2025 (UDI-DI 06971554720475), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971554720475 UDI-DI Date21 Feb 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  • Withdrawn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
InnoFine
Generic name
Needle guide, reusable
Model / reference
JSM-089
Primary DI / UDI-DI
06971554720475
FDA product code
OIJ
GMDN term
Needle guide, reusable
Device class
Class II
Regulation number
892.1560
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Needle guide, reusable.

Other devices from JingFang Precision Medical Device(Shenzhen) Co., Ltd.

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Properties

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