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Launch SLZ106

by Shenzhen Launch Electrical Co., Ltd

Ref SLZ106

Launch SLZ106 is a device classified as Class I in the EU and Class II in the US made by Shenzhen Launch Electrical Co., Ltd, registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 69474379ConnCableQC) and listed in FDA GUDID since 9 May 2020 (UDI-DI 06947437950147), 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 Number69474379ConnCableQC Basic UDI-DI 06947437950147UDI-DIDate23 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06947437950147 UDI-DI Date9 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 69474379ConnCableQC registered 23 Sep 2026 Active
  • FDA GUDID UDI-DI 06947437950147 listed 9 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 06947437950147
  2. Registered EUDAMED 69474379ConnCableQC

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  • Withdrawn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
SpO2 Adapter Cable EUDAMED
Launch GUDID
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
SLZ106
Primary DI / UDI-DI
06947437950147
Basic UDI-DI
69474379ConnCableQC
Direct marketing DI
06947437950147
FDA product code
IKD
EMDN code
Z1203020285 Multi-parameter monitors - consumables
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
890.1175
EU registration type
Standard device
EU market of registration
Germany
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: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under MULTI-PARAMETER MONITORS - CONSUMABLES.

Other devices from Shenzhen Launch Electrical Co., Ltd

See all devices from Shenzhen Launch Electrical Co., Ltd →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (21, all answered No)