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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

GNRB — Class IIa MDR by GENOUROB

MD Atlas
GENOUROB

EUDAMED last updated this device on Jan 19, 2026

GNRB

37012090LDAQ8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GENOUROB
UDI-DI code: 03701209000019
Reference / catalog number: GNRB

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Manufacturer information

Organization name: GENOUROB
SRN: FR-MF-000029224
Manufacturer status: Active

Critical warnings

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

CW016
EUDAMED did not publish a description for this code.
CW273
EUDAMED did not publish a description for this code.
CW011
For patients who have undergone anterior cruciate ligament surgery, follow the protocols in current use.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03701209000019
Basic UDI-DI: 37012090LDAQ8
Reference / catalog number: GNRB
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V030202GONIOMETERS

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

Dyneelax37012090LDAQ8On the market ROTAB37012090LDAQ8On the market ROTAM37012090LDAQ8On 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.