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Puritan Bennett

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Puritan Bennett FDA UDI
Generic Name
Neonatal/adult intensive-care ventilator FDA UDI
Device Name
980 Ventilator Compressor Configuration FDA UDI
Model / Reference
980X3ENDRAC FDA UDI
Description
980 Ventilator Compressor Configuration FDA UDI

Identifiers

Primary DI / UDI-DI
10884521172876 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Neonatal/adult intensive-care ventilator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Neonatal/adult intensive-care ventilator

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

Similar devices

Also classified as Neonatal/adult intensive-care ventilator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 5cef17db-29dd-4e4f-a543-42dcbd2c2888 35 fields · synced May 31, 2026