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Life Scope G9

FDA UDI

Class II (US FDA UDI)

by Nihon Kohden Corp.

Identity

Trade Name
Life Scope G9 FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
CORE UNIT - G9 (core i7 1.5GHz) FDA UDI
Model / Reference
CU-192R FDA UDI
Description
CORE UNIT - G9 (core i7 1.5GHz) FDA UDI

Identifiers

Catalog Number
CU-192RA FDA UDI
Primary DI / UDI-DI
04931921112168 FDA UDI
FDA Product Code
MHX FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: General-purpose multi-parameter bedside monitor

Life Scope G9 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 2c6d943c-9d52-4651-b526-b8f9314b3b33 35 fields · synced May 30, 2026