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Resp-O2 Oxygen Tubing Nut Nipple Adaptors

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Oxygen Tubing Nut Nipple Adaptors FDA UDI
Generic Name
Inhalation-therapy adaptor, single-use FDA UDI
Model / Reference
33307 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117318670 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Inhalation-therapy adaptor, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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: Inhalation-therapy adaptor, single-use

Resp-O2 Oxygen Tubing Nut Nipple Adaptors by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inhalation-therapy adaptor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI ef040f7e-142b-4cc5-a42a-c67baef64baf 32 fields · synced Jun 8, 2026