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Clear Arch Mobile

FDA UDI

Class I (US FDA UDI)

by Mobilehelp Llc

Identity

Trade Name
Clear Arch Mobile FDA UDI
Generic Name
Home healthcare information system application software FDA UDI
Device Name
Remote Patient Monitoring Application FDA UDI
Model / Reference
1 FDA UDI
Description
Remote Patient Monitoring Application FDA UDI

Identifiers

Primary DI / UDI-DI
00817644020185 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Home healthcare information system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home healthcare information system application software

Clear Arch Mobile by Mobilehelp Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home healthcare information system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mobilehelp Llc

Sources (1)

  • FDA UDI cb0acaf6-73ce-476d-a79f-35a6a5863dad 33 fields · synced Jun 6, 2026