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1009-C

by Tianjin Newtrans Technology Development

1009-C is a Class II device made by Tianjin Newtrans Technology Development, listed in FDA GUDID since 12 Jan 2023 (UDI-DI 16973881680009), registry data as of 8 Jun 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 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16973881680009 UDI-DI Date12 Jan 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  • Withdrawn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

Generic name
General-purpose surgical suction system, vacuum
Model / reference
1009-C
Primary DI / UDI-DI
16973881680009
FDA product code
KDQ
GMDN term
General-purpose surgical suction system, vacuum
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KDQ (Bottle, Collection, Vacuum).

Other devices from Tianjin Newtrans Technology Development

See all devices from Tianjin Newtrans Technology Development →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)