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cue-Rx

FDA UDI

Class I (US FDA UDI)

by One World Design And Manufacturing Group Ltd

Identity

Trade Name
cue-Rx FDA UDI
Generic Name
Personal pill dose dispenser, electric FDA UDI
Device Name
Medication management system FDA UDI
Model / Reference
1 FDA UDI
Description
Medication management system FDA UDI

Identifiers

Primary DI / UDI-DI
00860000925907 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal pill dose dispenser, electric

cue-Rx by One World Design And Manufacturing Group Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Personal pill dose dispenser, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8287f216-058c-476a-9239-c221954278c4 34 fields · synced May 31, 2026