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YiFang YF-001

by Shenzhen YI Fang Blister Packaging Co., Ltd.

YiFang YF-001 is a Class II device made by Shenzhen YI Fang Blister Packaging Co., Ltd., cleared under FDA 510(k) K240023 on 1 Mar 2024 and listed in FDA GUDID since 30 Aug 2024 (UDI-DI 06977488690006), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K240023

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06977488690006 UDI-DI Date30 Aug 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK240023 Date1 Mar 2024DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K240023 decided 1 Mar 2024 Active
  • FDA GUDID UDI-DI 06977488690006 listed 30 Aug 2024 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K240023
  2. Listed FDA GUDID 06977488690006

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
YiFang
Generic name
Electronic thermometer probe cover
Model / reference
YF-001
Primary DI / UDI-DI
06977488690006
510(k) Number
FDA product code
FLL
GMDN term
Electronic thermometer probe cover
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Electronic thermometer probe cover.

Other devices from Shenzhen YI Fang Blister Packaging Co., Ltd.

Properties

  • Single use
  • Expiration date
  • Manufacturing date
Other properties (12, all answered No)