← Back to catalogue

SimplyGo Mini

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
SimplyGo Mini FDA UDI
Generic Name
Mobile/portable oxygen concentrator FDA UDI
Device Name
SimplyGo Mini Portable Oxygen Concentrator, Brazil FDA UDI
Model / Reference
SimplyGo Mini, BR FDA UDI
Description
SimplyGo Mini Portable Oxygen Concentrator, Brazil FDA UDI

Identifiers

Catalog Number
1130731 FDA UDI
Primary DI / UDI-DI
00606959042070 FDA UDI
FDA Product Code
CAW FDA UDI
GMDN Term
Mobile/portable oxygen concentrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5440 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

SimplyGo Mini by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
Respironics, Inc.

Sources (1)

  • FDA UDI 4f3b0eb3-195d-47c9-998c-802c872e368c 37 fields · synced Jun 8, 2026