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Reusable Snap Lead Cable 1.0m (39"), (1.5mm DIN) Green, 1/pkg

by Natus Medical Incorporated Dba Excel-Tech Ltd (Xltek)

Part of a family of 9 devices: see the family page

Ref 1411516

Reusable Snap Lead Cable 1.0m (39"), (1.5mm DIN) Green, 1/pkg (1411516) is a device classified as Class I in the EU and Class II in the US made by Natus Medical Incorporated Dba Excel-Tech Ltd (Xltek), registered in EUDAMED on 4 Mar 2026 (Basic UDI-DI 00382830059015D8), cleared under FDA 510(k) K172703 on 13 Nov 2017 and listed in FDA GUDID since 29 Oct 2019 (UDI-DI 00382830025331), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K172703

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number00382830059015D8 Basic UDI-DI 00382830025331UDI-DIDate4 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00382830025331 UDI-DI Date29 Oct 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Abbreviated NumberK172703 Date13 Nov 2017DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 00382830059015D8 registered 4 Mar 2026 Active
  • FDA 510(k) K172703 decided 13 Nov 2017 Active
  • FDA GUDID UDI-DI 00382830025331 listed 29 Oct 2019 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K172703
  2. Listed FDA GUDID 00382830025331
  3. Registered EUDAMED 00382830059015D8

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Reusable Snap Lead Cable 1.0m (39"), (1.5mm DIN) Green, 1/pkg EUDAMED
Natus GUDID
Generic name
Polysomnograph
Device name
Natus Reusable Snap Leads and Natus Disposable Snap Electrodes
Model / reference
1411516
Primary DI / UDI-DI
00382830025331
Basic UDI-DI
00382830059015D8
Direct marketing DI
00382830025331
510(k) Number
FDA product code
GXY
EMDN code
Z12100380 Electroencephalography instruments - hardware accessories
GMDN term
Polysomnograph
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.1320
EU registration type
Standard device
EU market of registration
Ireland
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.

Manufacturer details

EUDAMED SRN
CA-MF-000004001
Authorised representative
Natus Manufacturing Ltd IE-AR-000000884

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Properties

  • Prescription use
  • Lot / batch number
Other properties (23, all answered No)