← Back to catalogue

Cadwell Sleepmate

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Cadwell Sleepmate FDA UDI
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling FDA UDI
Device Name
CannuTherm Adult Cannula with filter 84" FDA UDI
Model / Reference
302572-200-0484 FDA UDI
Description
CannuTherm Adult Cannula with filter 84" FDA UDI

Identifiers

Primary DI / UDI-DI
00709078013713 FDA UDI
FDA Product Code
CCK FDA UDI
CAT 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
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Cadwell Sleepmate by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 1650a697-d5a2-4dbe-b7b7-79982d3702e4 33 fields · synced Jun 1, 2026