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Ophthalmic Stool T-L

by Mdt Sp Z O O

Ref T-L

Ophthalmic Stool T-L is a Class I device made by Mdt Sp Z O O, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 5907642694STOJV) and listed in FDA GUDID since 16 Jul 2025 (UDI-DI 05907642694008), active as of 22 Oct 2026.

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

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5907642694STOJV Basic UDI-DI 05907642694008UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05907642694008 UDI-DI Date16 Jul 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 5907642694STOJV registered 19 May 2026 Active
  • FDA GUDID UDI-DI 05907642694008 listed 16 Jul 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05907642694008
  2. Registered EUDAMED 5907642694STOJV

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Taboret okulistyczny EUDAMED
Ophthalmic Stool GUDID
Generic name
General-purpose stool/chair
Device name
Ophthalmic Stool / Taboret okulistyczny
Model / reference
T-L
Primary DI / UDI-DI
05907642694008
Basic UDI-DI
5907642694STOJV
Direct marketing DI
05907642694008
FDA product code
HMG
EMDN code
Q0299 Ophthalmic devices - other
GMDN term
General-purpose stool/chair
Device class
Class I
Regulation number
886.1860
EU registration type
Standard device
EU market of registration
Poland
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose stool/chair

Similar devices in this category

Other devices filed under OPHTHALMIC DEVICES - OTHER.

Other devices from Mdt Sp Z O O

See all devices from Mdt Sp Z O O →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)