Nv Ultra Mirage

FDA UDI

Class I (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name: NV ULTRA MIRAGE FDA UDI
Generic Name: CPAP/BPAP nasal mask, reusable FDA UDI
Device Name: NV ULTRA MIRAGE MASK SYS SHLW FDA UDI
Model / Reference: 60406 FDA UDI
Description: NV ULTRA MIRAGE MASK SYS SHLW FDA UDI

Identifiers

Catalog Number: 60406 FDA UDI
Primary DI / UDI-DI: 00619498604067 FDA UDI
FDA Product Code: BYG FDA UDI
GMDN Term: CPAP/BPAP nasal mask, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5580 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: CPAP/BPAP nasal mask, reusable

Nv Ultra Mirage by Resmed Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Resmed Pty Ltd

Sources (1)

FDA UDI 971a9df6-5d54-4e18-8ec5-b481f6cce10e 36 fields · synced Jun 1, 2026