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Magnesium Xylidyl

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref MAGX-0230

by VitalScientific

Identity

Trade Name
MAGNESIUM XYLIDYL EUDAMEDFDA UDI
Generic Name
Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI
Device Name
MAGNESIUM XYLIDYL EUDAMED
Model / Reference
MAGX-0230 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
03701700829003 EUDAMEDFDA UDI
Basic UDI-DI
B-03701700829003 EUDAMED
EMDN Code
W01010306 MAGNESIUM EUDAMED
GMDN Term
Magnesium (Mg2+) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

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

Magnesium Xylidyl by Vitalscientific — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VitalScientific
EUDAMED SRN
FR-MF-000004722

Sources (2)

  • EUDAMED 064a96af-35fc-4678-9db4-6a9e6ac8ef2e 61 fields · synced Jul 24, 2026
  • FDA UDI 23179bf0-1ab9-491b-abb0-4a03a7a188e3 32 fields · synced May 29, 2026