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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

DIAMOND 4 — IVDR Class A IVDR by Tridema Engineering srl

MD Atlas
Tridema Engineering srl

EUDAMED last updated this device on May 22, 2026

DIAMOND 4

805792056Diamond4GF

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Tridema Engineering srl
UDI-DI code: 08057920560031
Reference / catalog number: DIAM2026

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View device family (Basic UDI)

Manufacturer information

Organization name: Tridema Engineering srl
SRN: IT-MF-000054318
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jan 1, 2026	Jul 12, 2042

Device identification

Trade name: DIAMOND 4
UDI-DI code: 08057920560031
Basic UDI-DI: 805792056Diamond4GF
Reference / catalog number: DIAM2026
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The Diamond 2 is a semiautomatic coagulometer, a high-performance analyzer with photo-optical clot detection. It performs all coagulation tests. The Diamond 2 has two highly sensitive photometers, with a light source provided by two solid-state three-wavelength emitters (405 nm, 450 nm, 630 nm), ensuring accurate and precise results.
Additional information URL: https://www.tridema.it/---ivd.html
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)08057920560031

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

W0202020101SEMI-AUTOMATED COAGULOMETERS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

Diamond805792056DiamondQNOn the market DIAMOND 2805792056Diamond2GBOn 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.