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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

TA1503026 — Class I MDR by Juvazquez S.L.

MD Atlas
Juvazquez S.L.

EUDAMED last updated this device on Apr 1, 2026

TA1503026

84350895JuvPnSLQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Juvazquez S.L.
UDI-DI code: 18435089532996
Reference / catalog number: TA1503026

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Manufacturer information

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

Related devices

TA053100084350895JuvPnSLQOn the market TA050150284350895JuvPnSLQOn the market TA180370384350895JuvPnSLQOn the market TA150400584350895JuvPnSLQOn the market TA160303684350895JuvPnSLQOn 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.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 18435089532996
Basic UDI-DI: 84350895JuvPnSLQ
Reference / catalog number: TA1503026
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: 300
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