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AirMini

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
AirMini FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
N20 CONNECTOR FOR AIRMINI FDA UDI
Model / Reference
38844 FDA UDI
Description
N20 CONNECTOR FOR AIRMINI FDA UDI

Identifiers

Catalog Number
38844 FDA UDI
Primary DI / UDI-DI
00619498388448 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

No

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

No

FDA UDI

Category: Ventilator breathing circuit, reusable

AirMini by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resmed Pty Ltd

Sources (1)

  • FDA UDI 86aa7ea5-db63-4503-8ab5-bcb2b853786b 36 fields · synced May 31, 2026