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Pointe Scientific, Inc. Magnesium

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. Magnesium FDA UDI
Generic Name
Magnesium (Mg2+) IVD, reagent FDA UDI
Device Name
Pointe Scientific, Inc. Magnesium Reagent is for the quantitative determination of magnesium in serum. Packaged for use on Olympus Analyzers. For in vitro diagnostic use only. 6 x 25ml, 6 x 25ml FDA UDI
Model / Reference
OM929-300 FDA UDI
Description
Pointe Scientific, Inc. Magnesium Reagent is for the quantitative determination of magnesium in serum. Packaged for use on Olympus Analyzers. For in vitro diagnostic use only. 6 x 25ml, 6 x 25ml FDA UDI

Identifiers

Catalog Number
OM929-300 FDA UDI
Primary DI / UDI-DI
00811727015099 FDA UDI
510(k) Number
K853592 FDA UDI
FDA Product Code
JGJ FDA UDI
GMDN Term
Magnesium (Mg2+) IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1495 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Magnesium (Mg2+) IVD, reagent

Pointe Scientific, Inc. Magnesium by Pointe Scientific, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnesium (Mg2+) IVD, reagent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6cb24a81-4ae0-4f79-8530-af0a95576df7 37 fields · synced Jun 6, 2026