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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

TONICROSS PLUS — Class I MDR by RUPIANI

MD Atlas
RUPIANI

EUDAMED last updated this device on Sep 30, 2023

TONICROSS PLUS

376032952TPLUS01994

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RUPIANI
UDI-DI code: 03760329520074
Reference / catalog number: TPU20

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Manufacturer information

Organization name: RUPIANI
SRN: FR-MF-000001715
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: TONICROSS PLUS
UDI-DI code: 03760329520074
Basic UDI-DI: 376032952TPLUS01994
Reference / catalog number: TPU20
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.rupiani.fr/fr/prods.php?id_prod=12&lang=fr&details=ok&table=ok&nav=2
Clinical sizes: 2

EMDN nomenclature code(s)

Y121806PEDAL TRICYCLES

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
Serial number
Software identification

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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.