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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

CaloPix 5.2.9 — IVDD — General IVDD by Tribun Health

MD Atlas
Tribun Health

EUDAMED last updated this device on May 4, 2026

CaloPix 5.2.9

B-FRMF000002560CPX529GD

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Tribun Health
UDI-DI code: D-FRMF000002560CPX529GD
Reference / catalog number: CaloPix 5.2.9

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Manufacturer information

Organization name: Tribun Health
SRN: FR-MF-000002560
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 12, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-FRMF000002560CPX529GD
Basic UDI-DI: B-FRMF000002560CPX529GD
Reference / catalog number: CaloPix 5.2.9
Issuing entity: EUDAMED

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic 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)

W0202050392LABORATORY INSTRUMENTS FOR MICROSCOPIC INVESTIGATIONS - IVD MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

CaloPix 5.2.10B-FRMF000002560CPX52106ROn the market CaloPix 5.2.12B-FRMF000002560CPX52126VOn the market CaloPix 5.2.13B-FRMF000002560CPX52136XOn 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.