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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

PC3DMXXXX — Class I MDR by FRANCEHOPITAL SAS

MD Atlas
FRANCEHOPITAL SAS

EUDAMED last updated this device on Jul 7, 2025

PC3DMXXXX

805577667PersocarPlusA8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FRANCEHOPITAL SAS
UDI-DI code: 08055776671222
Reference / catalog number: PC3DMXXXX

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Manufacturer information

Organization name: FRANCEHOPITAL SAS
SRN: FR-MF-000038034
Manufacturer status: Active

Related devices

CB40DMXXXX805577667CbPlus7YOn the market CB30DMXXXX805577667CbPlus7YOn the market CB10DMXXXX805577667CbPlus7YOn the market CB20DMXXXX805577667CbPlus7YOn the market ESDMXXXX805577667EssentialPlusGBOn 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.

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: 08055776671222
Basic UDI-DI: 805577667PersocarPlusA8
Reference / catalog number: PC3DMXXXX
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: CARRELLO PERSOCAR 3
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0899MEDICAL SUPPORT EQUIPMENT - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification