← Back to catalogue

RPSII-V2 Air10 PSU Adaptor

FDA UDI

Class II (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
RPSII-V2 Air10 PSU Adaptor FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Device Name
RPSII-V2 Air10 PSU Adaptor FDA UDI
Model / Reference
24706 FDA UDI
Description
RPSII-V2 Air10 PSU Adaptor FDA UDI

Identifiers

Catalog Number
24706 FDA UDI
Primary DI / UDI-DI
00619498247066 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable/mobile rechargeable battery pack

RPSII-V2 Air10 PSU Adaptor by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Resmed Pty Ltd

Sources (1)

  • FDA UDI 28691caa-d003-47c3-aa9e-e74d5db444ca 36 fields · synced May 31, 2026