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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

7144 — Class I MDR by ARTSANITY SRL

MD Atlas
ARTSANITY SRL

EUDAMED last updated this device on Oct 15, 2025

7144

805577665IMMSPALLARTSUPS7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ARTSANITY SRL
UDI-DI code: 08055776652658
Reference / catalog number: 7144

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View device family (Basic UDI)

Manufacturer information

Organization name: ARTSANITY SRL
SRN: IT-MF-000031338
Manufacturer status: Active

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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.

Critical warnings

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

CW030
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Feb 8, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08055776652658
Basic UDI-DI: 805577665IMMSPALLARTSUPS7
Reference / catalog number: 7144
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Tutore di spalla con fascia avvolgente e fasce di chiusura imbottite
Additional information URL: https://www.artsanity.it/
Clinical sizes: XL (Extra Large)

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08055776652658

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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.

M030501IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE

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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