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Pointe Scientific, Inc.

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. FDA UDI
Generic Name
Magnesium (Mg2+) IVD, reagent FDA UDI
Device Name
Reagent for the quantitative determination of magnesium in serum. 1 x 500ml, 4 x 15ml FDA UDI
Model / Reference
M7527-560 FDA UDI
Description
Reagent for the quantitative determination of magnesium in serum. 1 x 500ml, 4 x 15ml FDA UDI

Identifiers

Catalog Number
M7527-560 FDA UDI
Primary DI / UDI-DI
00811727013361 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. 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 f3db4f4b-162e-495a-a8c3-d67dd0b2a5e3 37 fields · synced Jun 8, 2026