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Smart Cable NMT Module and Accessories

FDA UDI

Class II (US FDA UDI)

by Nihon Kohden Corp.

Identity

Trade Name
Smart Cable NMT Module and Accessories FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Main cable FDA UDI
Model / Reference
JW-201P FDA UDI
Description
Main cable FDA UDI

Identifiers

Catalog Number
JW-201P FDA UDI
Primary DI / UDI-DI
04931921011089 FDA UDI
FDA Product Code
KOI FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2775 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose multi-parameter bedside monitor

Smart Cable NMT Module and Accessories by Nihon Kohden Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nihon Kohden Corp.

Sources (1)

  • FDA UDI 0327bb61-f369-4c5b-b9a3-a7156b7837e5 34 fields · synced May 30, 2026