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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

SENTANTE™ ENDOVASCULAR ROBOTIC… — Class IIb MDR

MD Atlas
UAB Inovatyvi Medicina

EUDAMED last updated this device on May 12, 2026

SENTANTE™ ENDOVASCULAR ROBOTIC SYSTEM

477906052SENTANTEF3

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: UAB Inovatyvi Medicina
UDI-DI code: 04779060520303
Reference / catalog number: SEN-SYS-01

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View device family (Basic UDI)

Manufacturer information

Organization name: UAB Inovatyvi Medicina
SRN: LT-MF-000041802
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
IFU must be read before use

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Market distribution

Primary placement in Lithuania; available across 1 country total.

Country	On market since	Until
LithuaniaPrimary placement		Still on market

Device identification

Trade name: SENTANTE™ ENDOVASCULAR ROBOTIC SYSTEM
UDI-DI code: 04779060520303
Basic UDI-DI: 477906052SENTANTEF3
Reference / catalog number: SEN-SYS-01
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The SENTANTE™ ENDOVASCULAR ROBOTIC SYSTEM is intended for use in the remote delivery and manipulation of commonly used and compatible catheter-based interventional devices (e.g., wires, sheaths, balloons, stents, coils, etc.) during arterial endovascular procedures. The complete SENTANTE system comprises the following main functional units: - Remote Workstation; - Bedside Unit; - Cart; and - Nurse’s Workstation
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)04779060520303

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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.

C0104020299PERIPHERAL ANGIOGRAPHY THERAPEUTIC 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

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Related devices

This device is not currently linked to any other device.

Certificates

Certificate health across this manufacturer's portfolio.

ECM26MDR004Issued
Quality management systemNotified body: 1282Expiry: May 11, 2031