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Gen2 G2N28903

by Surgix Medical LLC 2 variants

Gen2 G2N28903 is a Class II device made by Surgix Medical LLC, listed in FDA GUDID since 20 Oct 2022 (UDI-DI 00840343706500), 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 Number00840343706500 UDI-DI Date20 Oct 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  • Withdrawn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
Gen2
Generic name
Suction system catheter, general-purpose
Model / Ref / Catalog
G2N28903
Primary DI / UDI-DI
00840343706500
FDA product code
JOL
GMDN term
Suction system catheter, general-purpose
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 8 Inch
Catheter Gauge — 3 French

Related devices

Category: Suction system catheter, general-purpose

Other devices from Surgix Medical LLC

See all devices from Surgix Medical LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)