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Juneland 005

by Suzhou Juneland Medical Co., Ltd.

Juneland 005 is a Class II device made by Suzhou Juneland Medical Co., Ltd., listed in FDA GUDID since 11 Apr 2023 (UDI-DI 06976143660057), 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 Number06976143660057 UDI-DI Date11 Apr 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  • Withdrawn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

Trade name
Juneland
Generic name
Surgical mist irrigation tip
Model / reference
005
Primary DI / UDI-DI
06976143660057
FDA product code
JOL
GMDN term
Surgical mist irrigation tip
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JOL (Catheter And Tip, Suction).

Other devices from Suzhou Juneland Medical Co., Ltd.

See all devices from Suzhou Juneland Medical Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)