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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

DERMOJET — Class IIa MDD by AKRA DERMOJET

MD Atlas
AKRA DERMOJET

EUDAMED last updated this device on May 21, 2026

DERMOJET

B-3770035744DERMOJETWZ

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: AKRA DERMOJET
UDI-DI code: D-3770035744DERMOJETWZ
Reference / catalog number: 200

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Manufacturer information

Organization name: AKRA DERMOJET
SRN: FR-MF-000011748
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.

Country	On market since	Until
FrancePrimary placement	Jan 1, 1960	Still on market

Device identification

Trade name: DERMOJET
UDI-DI code: D-3770035744DERMOJETWZ
Basic UDI-DI: B-3770035744DERMOJETWZ
Reference / catalog number: 200
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: Injecteur sans aiguille
Additional information URL: https://dermojet.com/wp-content/uploads/2025/03/NOTICE-HR-FR-2025.pdf
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A020299REUSABLE SYRINGES - 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

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.