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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

Bimedoc Expert — Class I MDD by Bimedoc

MD Atlas
Bimedoc

EUDAMED last updated this device on Jun 1, 2026

Bimedoc Expert

B-03770026126011

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Bimedoc
UDI-DI code: 03770026126011
Reference / catalog number: Bimedoc Expert v1.62.0

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View device family (Basic UDI)

Manufacturer information

Organization name: Bimedoc
SRN: FR-MF-000008941
Manufacturer status: Active

Critical warnings

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

CW999
For professional use only: restricted to pharmacists (community or hospital), hospital pharmacy interns, and 6th-year pharmacy students
CW999
Bimedoc Expert is an informational tool. It does not replace the pharmacist's clinical judgment. Any therapeutic decision must be made by a qualified healthcare professional. Absence of alert does not guarantee absence of medication risk.
CW999
Alerts are generated based on user-entered patient data. Errors or omissions in data entry may result in absence of relevant alerts, generation of inappropriate alerts, or erroneous therapeutic management
CW999
No alerts are generated for pregnancy or lactation. The DDI Predictor component (third-party SOUP) may be updated without prior notice, potentially modifying results silently. Renal function values may not be accurate and must be verified clinically before any therapeutic decision

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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: Bimedoc Expert
UDI-DI code: 03770026126011
Basic UDI-DI: B-03770026126011
Reference / catalog number: Bimedoc Expert v1.62.0
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)03770026126011

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

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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.