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INOmax

FDA UDI

Class I (US FDA UDI)

by Mallinckrodt Manufacturing, LLC

Identity

Trade Name
INOmax FDA UDI
Generic Name
Nitric oxide delivery unit, system-based FDA UDI
Device Name
Evolve Bunnell Life Pulse Conv Pack with Natvar FDA UDI
Model / Reference
50383 FDA UDI
Description
Evolve Bunnell Life Pulse Conv Pack with Natvar FDA UDI

Identifiers

Primary DI / UDI-DI
00810055280117 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Nitric oxide delivery unit, system-based FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nitric oxide delivery unit, system-based

INOmax by Mallinckrodt Manufacturing, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitric oxide delivery unit, system-based.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6629f6ce-38e8-47c8-a948-d4000bf7c056 35 fields · synced Jun 6, 2026