Skip to content

TytoPro G2

by Tyto Care Ltd

Ref 900-00002-062Model G2

TytoPro G2 (900-00002-062) is a device classified as Class IIa in the EU and Class II in the US made by Tyto Care Ltd, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 07290016672TYTOPROVQ) and listed in FDA GUDID since 26 May 2024 (UDI-DI 07290016672756), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number07290016672TYTOPROVQ Basic UDI-DI 07290016672756UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07290016672756 UDI-DI Date26 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 07290016672TYTOPROVQ registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 07290016672756 listed 26 May 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07290016672756
  2. Registered EUDAMED 07290016672TYTOPROVQ

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  • Withdrawn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
TytoPro G2, Unified EUDAMED
TytoPro GUDID
Generic name
Multi-purpose digital medical camera
Model / Ref / Catalog
G2, 900-00002-062, TytoPro G2
Primary DI / UDI-DI
07290016672756
Basic UDI-DI
07290016672TYTOPROVQ
FDA product code
FLL, DQD, KYT, ERA
EMDN code
V0599 Clinical procedures kits not included in other classes - other
GMDN term
Multi-purpose digital medical camera
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
880.2910, 870.1875, 880.6350, 874.4770
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
A system/procedure pack comprising CE-marked Tyto Thermometer, Tyto Stethoscope, Tyto Otoscope and Tyto Exam Camera for use in accordance with the individual devices' intended purposes and instructions for use. The combined kit does not introduce a new intended purpose.
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
G2
900-00002-062
GUDID
TytoPro G2
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Infrared patient thermometer, skinOtoscope, directElectronic acoustic stethoscopeMulti-purpose digital medical camera

Similar devices in this category

Other devices filed under CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Tyto Care Ltd

See all devices from Tyto Care Ltd →

Properties

  • Over-the-counter
  • Convenience kit
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)