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Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
25' (7.6m) Crush Resistant Tubing, Adult Universal Connector FDA UDI
Model / Reference
33147 FDA UDI
Description
25' (7.6m) Crush Resistant Tubing, Adult Universal Connector FDA UDI

Identifiers

Primary DI / UDI-DI
00840117316331 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 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

Yes

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, basic

Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 34f24788-86e3-44b6-a56a-a8e44826f67a 33 fields · synced Jun 8, 2026