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Repair Parts

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
REPAIR PARTS FDA UDI
Generic Name
Mobile/portable oxygen concentrator FDA UDI
Device Name
O2 Conc Fitting Receptacle Port Invacare HomeFill #1104152 FDA UDI
Model / Reference
RP007 FDA UDI
Description
O2 Conc Fitting Receptacle Port Invacare HomeFill #1104152 FDA UDI

Identifiers

Primary DI / UDI-DI
00848530104641 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Mobile/portable oxygen concentrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile/portable oxygen concentrator

Repair Parts by SUNSET HEALTHCARE SOLUTIONS, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile/portable oxygen concentrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9e3d9f04-d360-4a85-af4a-e5dca9685256 33 fields · synced Jun 7, 2026