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Aircurve11 Vpap Tx

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
AIRCURVE11 VPAP TX FDA UDI
Generic Name
Home BPAP unit FDA UDI
Device Name
AIRCURVE11 VPAP TX TRI FDA UDI
Model / Reference
39024 FDA UDI
Description
AIRCURVE11 VPAP TX TRI FDA UDI

Identifiers

Primary DI / UDI-DI
00619498390243 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Home BPAP unit 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home BPAP unit

Aircurve11 Vpap Tx by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home BPAP unit.

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 c91a4d72-7ce1-4967-b1f6-c2836b70b68c 34 fields · synced May 31, 2026