← Back to catalogue

Puritan Bennett

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
Puritan Bennett FDA UDI
Generic Name
Breathing circuit multi-parameter sensor FDA UDI
Device Name
Proximal Flow Sensor Neonatal FDA UDI
Model / Reference
10047078 FDA UDI
Description
Proximal Flow Sensor Neonatal FDA UDI

Identifiers

Primary DI / UDI-DI
20884521210933 FDA UDI
FDA Product Code
BXP FDA UDI
GMDN Term
Breathing circuit multi-parameter sensor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2885 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

Yes

FDA UDI

Category: Breathing circuit multi-parameter sensor

Puritan Bennett by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing circuit multi-parameter sensor.

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
Covidien LP

Sources (1)

  • FDA UDI 2ab9e323-c3a6-49aa-9466-630d2d7ce45a 35 fields · synced Jun 8, 2026