← Back to catalogue

Unit Connection Cable, 1M YS-107P1

EUDAMEDFDA UDI

Class I (EU MDR)

Ref YS-107P1

by Nihon Kohden Corporation

Identity

Trade Name
Unit Connection Cable, 1M YS-107P1 EUDAMED
NA FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
General-purpose multi-parameter bedside monitor EUDAMED
Unit Connection Cable - G9 DAU FDA UDI
Model / Reference
YS-107P1 EUDAMEDFDA UDI
Description
Unit Connection Cable - G9 DAU FDA UDI

Identifiers

Catalog Number
YS-107P1 FDA UDI
Primary DI / UDI-DI
04931921112489 EUDAMEDFDA UDI
Basic UDI-DI
4931921MD10004BD EUDAMED
FDA Product Code
MHX FDA UDI
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose multi-parameter bedside monitor

Unit Connection Cable, 1M YS-107P1 by Nihon Kohden Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
JP-MF-000019022
Authorised Representative
NIHON KOHDEN EUROPE GmbH DE-AR-000010740

Sources (3)

  • EUDAMED 51b3d83a-5ac9-431e-b862-090a7b3d6758 61 fields · synced Jun 19, 2026
  • FDA UDI c38f5350-143d-4cd9-b7f1-2bba51157635 35 fields · synced May 30, 2026
  • EUDAMED e0d35683-0ddf-4b98-aa54-d5dd4f49fd43 61 fields · synced Jun 19, 2026