← Back to catalogue

CNS-9601 Serial Cable YS-094P2

EUDAMEDFDA UDI

Class I (EU MDR)

Ref YS-094P2

by Nihon Kohden Corporation

Identity

Trade Name
CNS-9601 Serial Cable YS-094P2 EUDAMED
NA FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
General-purpose multi-parameter bedside monitor EUDAMED
Serial cable (PIT cable) FDA UDI
Model / Reference
YS-094P2 EUDAMEDFDA UDI
Description
Serial cable (PIT cable) FDA UDI

Identifiers

Primary DI / UDI-DI
04931921120798 EUDAMEDFDA UDI
Basic UDI-DI
4931921MD10004BD EUDAMED
FDA Product Code
MHX FDA UDI
EMDN Code
Z1203020280,Z1203020285 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

CNS-9601 Serial Cable YS-094P2 by Nihon Kohden Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 (2)

  • EUDAMED 18e5804d-01c3-4bac-9edf-8f5bda63d78b 61 fields · synced Oct 6, 2026
  • FDA UDI a3aaa915-f50f-4622-a9c8-3a79f697750a 34 fields · synced May 30, 2026