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Tip Sucker 201080-000

by Novosci Corp.

Tip Sucker 201080-000 is a Class II device made by Novosci Corp., listed in FDA GUDID since 9 Oct 2015 (UDI-DI B0662010800000), 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 NumberB0662010800000 UDI-DI Date9 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Tip Sucker
Generic name
General-purpose surgical suction system, vacuum
Model / Ref / Catalog
201080-000
Primary DI / UDI-DI
B0662010800000
FDA product code
DTS
GMDN term
General-purpose surgical suction system, vacuum
Device class
Class II
Regulation number
870.4420
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DTS (Sucker, Cardiotomy Return, Cardiopulmonary Bypass).

Other devices from Novosci Corp.

See all devices from Novosci Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)