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Bypass electrodes Ag/AgCl

by Pamel d.o.o.

Part of a family of 7 devices: see the family page

Ref BYP10Model ELECUP120

Bypass electrodes Ag/AgCl (BYP10) is a device classified as Class I in the EU and Class II in the US made by PAMEL d.o.o., registered in EUDAMED on 7 Dec 2022 (Basic UDI-DI 385889415EEGELECTRODESHC), cleared under FDA 510(k) K211315 on 9 Nov 2021 and listed in FDA GUDID since 16 Aug 2023 (UDI-DI 03858894153398), 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) K211315

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number03858894153398 UDI-DI Date16 Aug 2023ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number385889415EEGELECTRODESHC Basic UDI-DI 03858894153398UDI-DIDate7 Dec 2022RegisteredStatusActive
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK211315 Date9 Nov 2021DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 385889415EEGELECTRODESHC registered 7 Dec 2022 Active
  • FDA 510(k) K211315 decided 9 Nov 2021 Active
  • FDA GUDID UDI-DI 03858894153398 listed 16 Aug 2023 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K211315
  2. Registered EUDAMED 385889415EEGELECTRODESHC
  3. Listed FDA GUDID 03858894153398

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  • Withdrawn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
Bypass electrodes Ag/AgCl EUDAMED
Comby EEG Cap GUDID
Generic name
Analytical scalp electrode, reusable
Device name
electrodes CUP 120cm with sintered Ag/AgCl electrodes
Model / Ref / Catalog
ELECUP120, BYP10, Bypass electrodes Ag/AgCl
Primary DI / UDI-DI
03858894153398
Basic UDI-DI
385889415EEGELECTRODESHC
510(k) Number
FDA product code
GXY
EMDN code
N01010203 EEG headsets
GMDN term
Analytical scalp electrode, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.1320
EU registration type
Standard device
EU market of registration
Croatia
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
ELECUP120
BYP10
GUDID
Bypass electrodes Ag/AgCl
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
HR-MF-000028336

Similar devices in this category

Other devices filed under ELECTROENCEPHALOGRAPHIC ELECTRODES.

Other devices from PAMEL d.o.o.

See all devices from PAMEL d.o.o. →

Properties

  • Reprocessed single-use device
  • Measuring function
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)