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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

MFL AS M01 — Class III MDD by MagForce NT GmbH

MD Atlas
MagForce NT GmbH

EUDAMED last updated this device on Oct 25, 2021

MFL AS M01

B-04251757400018

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: MagForce NT GmbH
UDI-DI code: 04251757400018
Reference / catalog number: MFL AS M01

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Manufacturer information

Organization name: MagForce NT GmbH
SRN: DE-MF-000007541
Manufacturer status: Inactive

Critical warnings

7 warnings recorded — scroll inside the panel to see all entries.

CW026
Keine Gefährdung für den Patienten, aber Beeinträchtigung des MRT-Bildes durch Artefakte im Bereich der Partikeldepots.
CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW036
Nur in Verbindung mit NanoTherm Therapiesystem.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Poland		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251757400018
Basic UDI-DI: B-04251757400018
Reference / catalog number: MFL AS M01
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

J99ACTIVE-IMPLANTABLE DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

MF-2223-0301-242517574CalTrolley001X8On the market

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.