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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

mint Lesion 3.10 — Class IIb MDR by Mint Medical GmbH

MD Atlas
Mint Medical GmbH

EUDAMED last updated this device on Sep 24, 2024

mint Lesion 3.10

426049588MINTLESIONSM

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mint Medical GmbH
UDI-DI code: 04260495883106
Reference / catalog number: mint Lesion 3.10

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Manufacturer information

Organization name: Mint Medical GmbH
SRN: DE-MF-000020202
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Sep 12, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260495883106
Basic UDI-DI: 426049588MINTLESIONSM
Reference / catalog number: mint Lesion 3.10
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 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)

Z11030582RADIOLOGY INSTRUMENTS - SOFTWARE ACCESSORIES

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

mint Lesion 3.12426049588MINTLESIONSMOn the market mint Lesion 3.11426049588MINTLESIONSMOn the market mint Lesion 3.9426049588MINTLESIONSMOn 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.