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Swivel Tubing Connector

FDA UDI

Class I (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
Swivel Tubing Connector FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
CONNECTOR SWIVEL TUBING FEMALE TO MALE FDA UDI
Model / Reference
R-3010 FDA UDI
Description
CONNECTOR SWIVEL TUBING FEMALE TO MALE FDA UDI

Identifiers

Catalog Number
R-3010 FDA UDI
Primary DI / UDI-DI
00628725097374 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, basic

Swivel Tubing Connector by Canadian Hospital Specialties Limited — 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

Sources (1)

  • FDA UDI 0e928c84-69de-45c6-9b81-4e4bfed74ad4 35 fields · synced May 30, 2026