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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

PRO MED — Class I MDR by DAMIANO S.R.L.

MD Atlas
DAMIANO S.R.L.

EUDAMED last updated this device on Sep 19, 2024

PRO MED

805848013PROMEDNH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DAMIANO S.R.L.
UDI-DI code: 08058480132027
Reference / catalog number: PRO MED

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View device family (Basic UDI)

Manufacturer information

Organization name: DAMIANO S.R.L.
SRN: IT-MF-000044162
Manufacturer status: Active

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ALL MED805848013ALLMEDDPOn the market ALL MED805848013ALLMEDDPOn the market ALL MED805848013ALLMEDDPOn the market ALL MED805848013ALLMEDDPOn the market LAY MED805848013LAYMEDH8On 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.

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: 08058480132027
Basic UDI-DI: 805848013PROMEDNH
Reference / catalog number: PRO MED
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: 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)08058480132027

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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.

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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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