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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

TA0502202 — Class I MDR by Juvazquez S.L.

MD Atlas
Juvazquez S.L.

EUDAMED last updated this device on Jul 8, 2022

TA0502202

84350895JuvPnSLQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Juvazquez S.L.
UDI-DI code: 18435089504719
Reference / catalog number: TA0502202

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Manufacturer information

Organization name: Juvazquez S.L.
SRN: ES-MF-000013941
Manufacturer status: Active

Related devices

TA150302684350895JuvPnSLQOn the market TA053100084350895JuvPnSLQOn the market TA050150284350895JuvPnSLQOn the market TA180370384350895JuvPnSLQOn the market TA150400584350895JuvPnSLQOn 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 Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 18435089504719
Basic UDI-DI: 84350895JuvPnSLQ
Reference / catalog number: TA0502202
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: 40
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0210NON-SURGICAL DRAPES

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