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Resp-O2 EtCO2 Nasal Sampling Cannula

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 EtCO2 Nasal Sampling Cannula FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
10' (3.0 m) Tubing, Female Luer Connector, Adult, Standard O2 Tubing Connector FDA UDI
Model / Reference
33191 FDA UDI
Description
10' (3.0 m) Tubing, Female Luer Connector, Adult, Standard O2 Tubing Connector FDA UDI

Identifiers

Primary DI / UDI-DI
00840117318823 FDA UDI
510(k) Number
K143150 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Resp-O2 EtCO2 Nasal Sampling Cannula by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, carbon-dioxide-sampling.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 80736760-6194-4639-81c1-f298a4477ab7 34 fields · synced May 30, 2026