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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

ROTAB — Class IIa MDR by GENOUROB

MD Atlas
GENOUROB

EUDAMED last updated this device on Jan 20, 2026

ROTAB

37012090LDAQ8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GENOUROB
UDI-DI code: 03701209000057
Reference / catalog number: ROTAB

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Manufacturer information

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

Related devices

Dyneelax37012090LDAQ8On the market GNRB37012090LDAQ8On the market ROTAM37012090LDAQ8On the market

Critical warnings

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

CW273
EUDAMED did not publish a description for this code.
CW016
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: 03701209000057
Basic UDI-DI: 37012090LDAQ8
Reference / catalog number: ROTAB
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

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.