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Dispo-Med

FDA UDI

Class II (US FDA UDI)

by Dispo-Med (malaysia) Sdn. Bhd.

Identity

Trade Name
Dispo-Med FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
CO2 Sampling Line, MLL, Tube 10FT FDA UDI
Model / Reference
DM-7100/CO-10FTM FDA UDI
Description
CO2 Sampling Line, MLL, Tube 10FT FDA UDI

Identifiers

Primary DI / UDI-DI
09555866300814 FDA UDI
510(k) Number
K143127 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dispo-Med by Dispo-Med (malaysia) Sdn. Bhd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e988db3-08aa-4686-ae35-de65e79ad4b4 35 fields · synced May 30, 2026