EUDAMED last updated this device on Jul 9, 2026

PLATINIUM CRT-D 1741

B-08031527014418

On the marketAIMDD

Applicable legislation: —
Organization name: MicroPort CRM S.r.l.
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 08031527014418
Reference / catalog number: TDF037C

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

PLATINIUM CRT-D 1741 is an AIMDD-legacy active implantable device registered in EUDAMED. It is classified as AIMDD. Manufactured by MicroPort CRM S.r.l.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: PLATINIUM CRT-D 1741
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 08031527014418
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-08031527014418
Reference / catalog number: TDF037C
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: AIMDD
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: PLATINIUM CRT-D is an implantable cardioverter defibrillator for the recognition and treatment of ventricular tachycardia and fibrillation, with ventricular resynchronization, in patients with spontaneous or inducible tachyarrhythmias. PLATINIUM CRT-D is equipped with an accelerometer to allow adaptation of pacing to suit the patient’s activity.
Additional information URL: https://www.microportmanuals.com/
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)08031527014418

EMDN nomenclature code(s)

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

J01050301IMPLANTABLE TRIPLE CHAMBER DEFIBRILLATORS, WITH SENSORS

Critical warnings

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

Consult instructions for use
Do not re-use
Do not resterilize
Do not use if package is damaged

Compliance flags

Safety

Reprocessed single-use

Direct marking

Substances

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Italy; available across 6 countries total.

Country	On market since	Until
ItalyPrimary placement	—	Still on market
Austria	—	Still on market
Czechia	—	Still on market
Germany	—	Still on market
Netherlands	—	Still on market
Türkiye	—	Still on market

PLATINIUM CRT-D 1741

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UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

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Regulatory

Lifecycle

Market distribution

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Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Legacy certificates

Certificates covering this device

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Manufacturer information

Certificates covering this device

Legacy certificates

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