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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

NEOGRAFT 2.0 — Class IIa MDR by ELECTRONIQUE DU MAZET

MD Atlas
ELECTRONIQUE DU MAZET

EUDAMED last updated this device on May 31, 2022

NEOGRAFT 2.0

137013302MED011KP1XXSQ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ELECTRONIQUE DU MAZET
UDI-DI code: 03701330200005
Reference / catalog number: MED011

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Manufacturer information

Organization name: ELECTRONIQUE DU MAZET
SRN: FR-MF-000001805
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Mar 17, 2026
Spain		Mar 17, 2026

Device identification

Trade name: NEOGRAFT 2.0
UDI-DI code: 03701330200005
Basic UDI-DI: 137013302MED011KP1XXSQ
Reference / catalog number: MED011
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

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

EMDN nomenclature code(s)

K0199ENDOTHERAPY 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

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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.