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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

PX16108 — Class I MDR by PRAXIS MEDICAL NETWORK…

MD Atlas
PRAXIS MEDICAL NETWORK SRL

EUDAMED last updated this device on Dec 20, 2021

PX16108

805848176020473

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRAXIS MEDICAL NETWORK SRL
UDI-DI code: 08058481760618
Reference / catalog number: PX16108

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View device family (Basic UDI)

Manufacturer information

Organization name: PRAXIS MEDICAL NETWORK SRL
SRN: IT-MF-000017626
Manufacturer status: Active

Related devices

PX16110805848176020473On the market PX1800480584817604047DOn the market PX18A0880584817604087MOn the market PX18A1180584817604117AOn the market PX16123805848176020677On 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: 08058481760618
Basic UDI-DI: 805848176020473
Reference / catalog number: PX16108
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

EMDN nomenclature code(s)

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

V0805030101MANUAL MOBILE LIFTS

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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