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Kabel EKG do badań holterowskich

by SORIMEX Sp. z o.o. 79 variants

Ref KH-5/0-Ha/0-G17a/L-60/120-52, KM-7/0-0/L-80-72, KS-22/0-5Hb/0-Inn/L-XLarge-22X, KS-2/0-G1/0-GDIN180/L-210-21, KH-4/0-H/0e-USBCb/L-9/18/57-41, KH-10/0-8/10-HDMI3e/L-80/100/120-IEC, 1-5-CU3, KH-5/0-Ha/0-0/L-60/83-51, KS-4/0-H/0e-Rf/300k/L-60/70-41, KS-4/0-Hb/10-MT101a/L-80/100-45, KH-7/0-Hb/0-HDMI3d/L-80/20-71, KH-5/0-H/0-K15c/L-70/40-51, KH-5/0-Ha/0-CU3/L-60/80-51, KH-3/0-Ha/0-0/L-50/50-31D, KH-10/0-8/0-FD14a/L-50/40-IEC, KH-5/0-H/0-0/L-50/30-51, 1-3-CF, KH-3/w-B1/0-PAG05/L-45/130-32A, KS-3/0-Hd/0e-H/0e-USBCe/L-60-301, KH-7/0-H/0e-G17c/L-27/150-72, KH-4/0-H/0e-MED4/L-70/35-44, KH-2/0-Ha/0-0/L-18/32-905, KH-5/0-Ha/0-0/L-40/60-51, KH-5/0-M/0-LA10d/L-30/70-51, KH-3/w-1/0-PAG05/L-45/130-32A, 1-3-NT, KS-22/0-5Hb/0-Inn/L-XSmall-22X, 1-5-G17, KS-2/0-1/0-DIN180/L-20/150-300, KH-2/0-H/0-HPs/L-60/20-121, KS-5/0-H/0e-Rm/L-65-51, KH-7/0-Ha/0-G17c/L-60/120-72, KS-22/0-5Hb/0-RDB37/L-Large-22X, KS-7/0-H/0e-A9/L-90-73, KH-10/0-H/0e-GCM12/L-31/39/44/49/54/74/79/15, KH-10/i-Hb/10-HDMI3e/L-80/100/20-IEC, KH-7/0-H/0e-Bs/1/L-40/20-72, KH-3/w(NAT)-1-PAG05/L-45/130-32A, 1-10-G17, 1-5-MT, 1-5-CU2, KH-5/0-Ha/0-MED7/L-60/80-51, KH-5/0-Hb/0-HDMI3b/L-40/10-51, KH-7/0-H/0e-Bs/1/L-50/40-72, KH-3/0-Ha/0-0/L-45/35-31, 15-5-0, KH-10/0-Hb/10-AM14c/L-120/250-AHA, KH-7-H-0/L-46/92-71, KH-7/0-Ha/0-MD15a/L-46/92-71, KH-7/0-H/0-0/L-50/50-72, 1-3-CF/C

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5903002221095N Basic UDI-DI Date8 May 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Holter ECG cables
Model / Reference
KH-5/0-Ha/0-G17a/L-60/120-52, KM-7/0-0/L-80-72, KS-22/0-5Hb/0-Inn/L-XLarge-22X, KS-2/0-G1/0-GDIN180/L-210-21, KH-4/0-H/0e-USBCb/L-9/18/57-41, KH-10/0-8/10-HDMI3e/L-80/100/120-IEC, 1-5-CU3, KH-5/0-Ha/0-0/L-60/83-51, KS-4/0-H/0e-Rf/300k/L-60/70-41, KS-4/0-Hb/10-MT101a/L-80/100-45, KH-7/0-Hb/0-HDMI3d/L-80/20-71, KH-5/0-H/0-K15c/L-70/40-51, KH-5/0-Ha/0-CU3/L-60/80-51, KH-3/0-Ha/0-0/L-50/50-31D, KH-10/0-8/0-FD14a/L-50/40-IEC, KH-5/0-H/0-0/L-50/30-51, 1-3-CF, KH-3/w-B1/0-PAG05/L-45/130-32A, KS-3/0-Hd/0e-H/0e-USBCe/L-60-301, KH-7/0-H/0e-G17c/L-27/150-72, KH-4/0-H/0e-MED4/L-70/35-44, KH-2/0-Ha/0-0/L-18/32-905, KH-5/0-Ha/0-0/L-40/60-51, KH-5/0-M/0-LA10d/L-30/70-51, KH-3/w-1/0-PAG05/L-45/130-32A, 1-3-NT, KS-22/0-5Hb/0-Inn/L-XSmall-22X, 1-5-G17, KS-2/0-1/0-DIN180/L-20/150-300, KH-2/0-H/0-HPs/L-60/20-121, KS-5/0-H/0e-Rm/L-65-51, KH-7/0-Ha/0-G17c/L-60/120-72, KS-22/0-5Hb/0-RDB37/L-Large-22X, KS-7/0-H/0e-A9/L-90-73, KH-10/0-H/0e-GCM12/L-31/39/44/49/54/74/79/15, KH-10/i-Hb/10-HDMI3e/L-80/100/20-IEC, KH-7/0-H/0e-Bs/1/L-40/20-72, KH-3/w(NAT)-1-PAG05/L-45/130-32A, 1-10-G17, 1-5-MT, 1-5-CU2, KH-5/0-Ha/0-MED7/L-60/80-51, KH-5/0-Hb/0-HDMI3b/L-40/10-51, KH-7/0-H/0e-Bs/1/L-50/40-72, KH-3/0-Ha/0-0/L-45/35-31, 15-5-0, KH-10/0-Hb/10-AM14c/L-120/250-AHA, KH-7-H-0/L-46/92-71, KH-7/0-Ha/0-MD15a/L-46/92-71, KH-7/0-H/0-0/L-50/50-72, 1-3-CF/C
Primary DI / UDI-DI
05908212625613, 05903002200223, 05903002206607, 05908212626313, 05903002208427, 05903002216859, 05908212626849, 05908212625576, 05903002215210, 05908212625675, 05903002216873, 05903002205341, 05908212626832, 05903002202586, 05908212625651, 05903002204917, 05908212626825, 05903002205297, 05903002215920, 05903002213995, 05903002212691, 05903002210932, 05908212629963, 05908212628393, 05903002203354, 05908212626672, 05903002206577, 05903002206454, 05908212626320, 05903002204146, 05903002200902, 05903002205235, 05903002208021, 05908212626467, 05903002200674, 05903002215883, 05908212624470, 05903002205402, 05903002206683, 05903002204153, 05903002200735, 05908212625590, 05903002216705, 05908212624463, 05903002204283, 05903002202838, 05903002211793, 05908212629192, 05903002201114, 05903002204931, 05908212627310
Basic UDI-DI
5903002221095N
EMDN Code
C020599, Z12050380, Z12050480
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000020958

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No