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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

400 — Class I MDR by POVATEX DI PREITE VITA…

MD Atlas
POVATEX DI PREITE VITA E C. s.a.s.

EUDAMED last updated this device on Feb 27, 2026

400

805596519404HG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: POVATEX DI PREITE VITA E C. s.a.s.
UDI-DI code: 08055965194006
Reference / catalog number: 400

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View device family (Basic UDI)

Manufacturer information

Organization name: POVATEX DI PREITE VITA E C. s.a.s.
SRN: IT-MF-000035313
Manufacturer status: Active

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: 08055965194006
Basic UDI-DI: 805596519404HG
Reference / catalog number: 400
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: Tutore ortopedico pediatrico indicato per il Trattamento di media e grave entità della Displasia Evolutiva dell'Anca (DEA) e Lussazione (per i tipi di anche: IIc, IIa e IIb della Classificazione di Graf). MISURA 0 :per una divaricazione indicativa di 14-16 cm e torace 32/36 cm. MATERIALI: Esterno: 100% Cotone anallergico e traspirante. Interno: Polietilene rigido con forma anatomica per garantire stabilità, combinato con imbottitura in materiale morbido espanso (Eva Form) per il massimo comfort.
Additional information URL: https://www.povatex.it/prodotto/salopette-correttiva-gio/
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)08055965194006

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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.

V0299NEONATOLOGY AND PAEDIATRIC DEVICES - 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

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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.