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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

MG1-10T6 — IVDD — General IVDD by METAFORA biosystems

MD Atlas
METAFORA biosystems

EUDAMED last updated this device on Apr 22, 2022

MG1-10T6

B-03770026177006

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: METAFORA biosystems
UDI-DI code: 03770026177006
Reference / catalog number: MG1-10T6

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Manufacturer information

Organization name: METAFORA biosystems
SRN: FR-MF-000004551
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03770026177006
Basic UDI-DI: B-03770026177006
Reference / catalog number: MG1-10T6
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: METAglut1™ is an in vitro diagnostic medical device (IVDMD) used to aid in the diagnosis of the GLUT1 Deficiency Syndrome (GLUT1-DS, or De Vivo disease)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103080699REAGENTS FOR FLOW CYTOMETRY - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Manufacturing date
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Software identification

Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.