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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

AD0RA744 — Class I MDR by RAM Apparecchi Medicali…

MD Atlas
RAM Apparecchi Medicali srl

EUDAMED last updated this device on Nov 15, 2021

AD0RA744

805188221BASTONIKC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RAM Apparecchi Medicali srl
UDI-DI code: 08051882210119
Reference / catalog number: AD0RA744

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View device family (Basic UDI)

Manufacturer information

Organization name: RAM Apparecchi Medicali srl
SRN: IT-MF-000015826
Manufacturer status: Active

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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: 08051882210119
Basic UDI-DI: 805188221BASTONIKC
Reference / catalog number: AD0RA744
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: Stampella avambraccio leggere tipo canadese, costruite in tubo di alluminio anodizzato. Impugnatura anatomica antiscivolo stampata ad iniezione e composta da un’unica parte per offrire comfort e sicurezza.
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

EMDN nomenclature code(s)

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

Y12030601ELBOW CRUTCHES

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

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.