Stellar

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name: Stellar FDA UDI
Generic Name: Portable electric ventilator FDA UDI
Device Name: Stellar filter - hypoallergen - 12 pack FDA UDI
Model / Reference: 24934 FDA UDI
Description: Stellar filter - hypoallergen - 12 pack FDA UDI

Identifiers

Catalog Number: 24934 FDA UDI
Primary DI / UDI-DI: 00619498249343 FDA UDI
FDA Product Code: MNT FDA UDI
GMDN Term: Portable electric 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable electric ventilator

Stellar by Resmed Pty Ltd — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Resmed Pty Ltd

Sources (1)

FDA UDI bcd27e6c-6e70-40dd-b0d0-54d2eda601fd 36 fields · synced May 30, 2026