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cap-ONE

FDA UDI

Class I (US FDA UDI)

by Nihon Kohden Corp.

Identity

Trade Name
cap-ONE FDA UDI
Generic Name
Carbon dioxide monitor FDA UDI
Device Name
Adult Cap-ONE Biteblock FDA UDI
Model / Reference
YG-227T FDA UDI
Description
Adult Cap-ONE Biteblock FDA UDI

Identifiers

Primary DI / UDI-DI
14931921904043 FDA UDI
FDA Product Code
MNK FDA UDI
GMDN Term
Carbon dioxide monitor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Carbon dioxide monitor

cap-ONE by Nihon Kohden Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide 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 e8dc8f15-a2f6-4d37-b14a-c5bf578a0c3d 34 fields · synced May 30, 2026