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Medsuresystems

FDA UDI

Class I (US FDA UDI)

by Lockedbrands LLC

Identity

Trade Name
Medsuresystems FDA UDI
Generic Name
Personal pill dose dispenser, electric FDA UDI
Device Name
aMed Device ver01 FDA UDI
Model / Reference
aMed Device ver01 FDA UDI
Description
aMed Device ver01 FDA UDI

Identifiers

Primary DI / UDI-DI
00860010414811 FDA UDI
FDA Product Code
NXQ 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal pill dose dispenser, electric

Medsuresystems by Lockedbrands LLC — 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

Manufacturer
Lockedbrands LLC

Sources (1)

  • FDA UDI 88121457-b75d-4a40-9053-a01590411cff 33 fields · synced May 30, 2026