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MP Biomedicals LLC

FDA UDI

Class I (US FDA UDI)

by Mp Biomedicals, Llc

Identity

Trade Name
MP Biomedicals LLC FDA UDI
Generic Name
Galactose IVD, kit, enzyme fluorescence FDA UDI
Device Name
NEONATAL GALACTOSE MW 2 PLATE ENZYME ASSAY KIT (WITH MEMBRANE) FDA UDI
Model / Reference
07553303 FDA UDI
Description
NEONATAL GALACTOSE MW 2 PLATE ENZYME ASSAY KIT (WITH MEMBRANE) FDA UDI

Identifiers

Catalog Number
07553303 FDA UDI
Primary DI / UDI-DI
00817830023105 FDA UDI
510(k) Number
K951329 FDA UDI
FDA Product Code
JIA FDA UDI
GMDN Term
Galactose IVD, kit, enzyme fluorescence FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1310 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Galactose IVD, kit, enzyme fluorescence

MP Biomedicals LLC by Mp Biomedicals, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Galactose IVD, kit, enzyme fluorescence.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mp Biomedicals, Llc

Sources (1)

  • FDA UDI 9050b324-00c2-4623-b0c3-f9fb2ad3114b 35 fields · synced May 30, 2026