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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

00100005 — Class I MDR by QUIROSA, S.A.

MD Atlas
QUIROSA, S.A.

EUDAMED last updated this device on Sep 15, 2022

00100005

84295551010CONEXIONESRB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: QUIROSA, S.A.
UDI-DI code: 08429555300052
Reference / catalog number: 00100005

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Manufacturer information

Organization name: QUIROSA, S.A.
SRN: ES-MF-000014841
Manufacturer status: Active

Related devices

0010000984295551010CONEXIONESRBOn the market 0010000884295551010CONEXIONESRBOn the market 0010010884295551010CONEXIONESRBOn the market 0010001384295551010CONEXIONESRBOn the market 0010000784295551010CONEXIONESRBOn 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.

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: 08429555300052
Basic UDI-DI: 84295551010CONEXIONESRB
Reference / catalog number: 00100005
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: 100
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10 x 10

EMDN nomenclature code(s)

A070101SUCTION TUBING ADAPTERS AND CONNECTORS

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