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Thora-Vent Thoracic Vent TVST

by Uresil Corp.

Ref TVST

Thora-Vent Thoracic Vent TVST is a device classified as Class I in the EU and Class II in the US made by Uresil Corp., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-00817640020806) and listed in FDA GUDID since 3 Jun 2022 (UDI-DI 00817640020806), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00817640020806 Basic UDI-DI 00817640020806UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00817640020806 UDI-DI Date3 Jun 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00817640020806 registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00817640020806 listed 3 Jun 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00817640020806
  2. Registered EUDAMED B-00817640020806

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Thora-Vent EUDAMED
Thora-Vent Thoracic Vent GUDID
Generic name
Pneumothorax catheter insertion set
Device name
Suction Tubing Set
Model / Ref / Catalog
TVST
Primary DI / UDI-DI
00817640020806
Basic UDI-DI
B-00817640020806
FDA product code
KDQ
EMDN code
A0680 Drainage and fluid collection devices - accessories
GMDN term
Pneumothorax catheter insertion set
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Pneumothorax catheter insertion set

Similar devices in this category

Other devices filed under DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES.

Other devices from Uresil Corp.

See all devices from Uresil Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)