← Back to catalogue

Cadwell

FDA UDI

Class II (US FDA UDI)

by Cadwell Industries, Inc.

Identity

Trade Name
Cadwell FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
Snore Microphone FDA UDI
Model / Reference
302556-200-9080 FDA UDI
Description
Snore Microphone FDA UDI

Identifiers

Primary DI / UDI-DI
00840067103364 FDA UDI
510(k) Number
K941759 FDA UDI
FDA Product Code
BZQ FDA UDI
GMDN Term
Home-use sleep apnoea recording system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Dimensions & Sizes

Size
Length — 200 Centimeter FDA UDI

Category: PolysomnographHome-use sleep apnoea recording system

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

Similar devices

Also classified as Home-use sleep apnoea recording system.

Cleared under the same submission

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

Sources (1)

  • FDA UDI a4e5a37d-92d5-4f60-9721-21170dedf95b 36 fields · synced Jun 9, 2026