Dosentrx Ltd

FDA UDI

Class I (US FDA UDI)

by Dosentrx Ltd

Identity

Trade Name: Dosentrx Ltd FDA UDI
Generic Name: Personal pill dose dispenser, electric FDA UDI
Device Name: ReX™ empowers you on your journey to better health. It is your personal companion that keeps you connected with your care team. FDA UDI
Model / Reference: ReX Companion FDA UDI
Description: ReX™ empowers you on your journey to better health. It is your personal companion that keeps you connected with your care team. FDA UDI

Identifiers

Catalog Number: ReX-C-2 FDA UDI
Primary DI / UDI-DI: 07290018680001 FDA UDI
FDA Product Code: NXB FDA UDI
GMDN Term: Personal pill dose dispenser, electric FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal pill dose dispenser, electric

Dosentrx Ltd by Dosentrx Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dosentrx Ltd

Sources (1)

FDA UDI ded8c573-63ff-4892-917d-ed06c5b21557 36 fields · synced May 30, 2026