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Diamedix

FDA UDI

Class I (US FDA UDI)

by Diamedix Corp.

Identity

Trade Name
Diamedix FDA UDI
Generic Name
Multichannel clinical chemistry analyser IVD, point-of-care, line-powered FDA UDI
Device Name
Mago 4S Anayzer FDA UDI
Model / Reference
MAGO 4S FDA UDI
Description
Mago 4S Anayzer FDA UDI

Identifiers

Primary DI / UDI-DI
00817273020471 FDA UDI
FDA Product Code
JJF FDA UDI
GMDN Term
Multichannel clinical chemistry analyser IVD, point-of-care, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2170 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multichannel clinical chemistry analyser IVD, point-of-care, line-powered

Diamedix by Diamedix Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multichannel clinical chemistry analyser IVD, point-of-care, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diamedix Corp.

Sources (1)

  • FDA UDI eb02b9ad-0663-4d6c-b9c5-82b086ffbaf6 35 fields · synced Jun 8, 2026