← Back to catalogue

Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline Industries, Inc. FDA UDI
Generic Name
Exhaled-gas oesophageal intubation detector FDA UDI
Device Name
INDICATOR,CO2,F/MANUAL RESUSCITATOR FDA UDI
Model / Reference
CPRMCO2 FDA UDI
Description
INDICATOR,CO2,F/MANUAL RESUSCITATOR FDA UDI

Identifiers

Catalog Number
CPRMCO2 FDA UDI
Primary DI / UDI-DI
10884389125960 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Exhaled-gas oesophageal intubation detector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exhaled-gas oesophageal intubation detector

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

Similar devices

Also classified as Exhaled-gas oesophageal intubation detector.

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
Medline Industries, Inc.

Sources (1)

  • FDA UDI 76494f0b-8276-4c0a-a45c-8158e2a39038 35 fields · synced Jun 1, 2026