← Back to catalogue

Pointe Magnesium Reagent

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Magnesium Reagent FDA UDI
Generic Name
Magnesium (Mg2+) IVD, reagent FDA UDI
Device Name
Pointe Magnesium Reagent packaged for use on the Mindray BS480. 6 x 20ml R1, 6 x 20ml R2. For the quantitative determination of magnesium in serum. For in vitro diagnostic use only. FDA UDI
Model / Reference
14-HM929-240 FDA UDI
Description
Pointe Magnesium Reagent packaged for use on the Mindray BS480. 6 x 20ml R1, 6 x 20ml R2. For the quantitative determination of magnesium in serum. For in vitro diagnostic use only. FDA UDI

Identifiers

Catalog Number
14-HM929-240 FDA UDI
Primary DI / UDI-DI
00811727015938 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 Magnesium Reagent 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 89e2f434-ad91-4173-94c1-d0a73685fd17 37 fields · synced May 30, 2026