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DE370

by Firefly Global

Ref DE370

DE370 is a Class I device made by Firefly Global, registered in EUDAMED on 2 Jan 2026 (Basic UDI-DI 0851289007DE370QL) and listed in FDA GUDID since 13 Feb 2020 (UDI-DI 00851289007118), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0851289007DE370QL Basic UDI-DI 00851289007118UDI-DIDate2 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00851289007118 UDI-DI Date13 Feb 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0851289007DE370QL registered 2 Jan 2026 Active
  • FDA GUDID UDI-DI 00851289007118 listed 13 Feb 2020 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 00851289007118
  2. Registered EUDAMED 0851289007DE370QL

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  • Withdrawn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
Firefly
Generic name
Dermatoscope, digital
Model / reference
DE370
Primary DI / UDI-DI
00851289007118
Basic UDI-DI
0851289007DE370QL
FDA product code
KYT
EMDN code
Z12040108 Dermatoscopes
GMDN term
Dermatoscope, digital
Device class
Class I
Regulation number
880.6350
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
US-MF-000020015
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under DERMATOSCOPES.

Other devices from Firefly Global

See all devices from Firefly Global →

Properties

  • Single use
  • Premarket exempt
  • Serial number
Other properties (22, all answered No)