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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

P344300000 — Class I MDR by Capsulit spa

MD Atlas
Capsulit spa

EUDAMED last updated this device on Mar 30, 2026

P344300000

8050593770000000018R

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Capsulit spa
UDI-DI code: 08050593770837
Reference / catalog number: P344300000

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View device family (Basic UDI)

Manufacturer information

Organization name: Capsulit spa
SRN: IT-MF-000013452
Manufacturer status: Active

Related devices

P32010H0008050593770000000018ROn the market P3206000008050593770000000018ROn the market P3444000008050593770000000018ROn the market P3441000008050593770000000018ROn the market P3432000008050593770000000018ROn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08050593770837
Basic UDI-DI: 8050593770000000018R
Reference / catalog number: P344300000
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: —
Additional information URL: http://www.capsulit.it/misurini-e-cucchiaini-dosatori-consigli-per-lutilizzatore/
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)08050593770837

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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.

V0499CLINICAL USE CONTAINERS (NON-IVD) - 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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Certificates

Certificate health across this manufacturer's portfolio.

55391Issued
Quality management systemNotified body: 0546Expiry: Aug 8, 2027