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Sample, Lighted Suction Handle 22625

by Bionix, LLC

Sample, Lighted Suction Handle 22625 is an ear canal suction handle (FDA Class I; FDA product code JZF, Tube, Ear Suction) made by Bionix, LLC, listed in FDA GUDID since 10 Jul 2024 (UDI-DI 00714646001085), 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 Number00714646001085 UDI-DI Date10 Jul 2024ListedStatusListed 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  • Withdrawn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
Sample, Lighted Suction Handle
Generic name
Ear canal suction handle
Model / Ref / Catalog
22625
Primary DI / UDI-DI
00714646001085
FDA product code
JZF
GMDN term
Ear canal suction handle
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ear canal suction handle

Similar devices

Other devices filed under FDA product code JZF (TUBE, EAR SUCTION).

Other devices from Bionix, LLC

See all devices from Bionix, LLC →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)