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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

1800 — Class I MDR by Rovipharm

MD Atlas
Rovipharm

EUDAMED last updated this device on Jan 5, 2026

1800

3666663PDOS8V

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rovipharm
UDI-DI code: 03760337566521
Reference / catalog number: 1800

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Manufacturer information

Organization name: Rovipharm
SRN: FR-MF-000000673
Manufacturer status: Active

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26130101376033756PIBADQOn the market réducteur PF PP28 glass CE376033756PIBADQOn the market réducteur PF PP28 glass CE ENS376033756PIBADQOn the market Réglette Bronchodermine BL CE3666663REDOS53On the market 266368713666663PDOS8VOn 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.

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.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03760337566521
Basic UDI-DI: 3666663PDOS8V
Reference / catalog number: 1800
Issuing entity: GS1

Classification

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

Device details

Quantity: 1800
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)

V0399MEASUREMENT 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
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Software identification