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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

92501015 — Class I MDR by Material clínico y…

MD Atlas
Material clínico y sanitario, S.L

EUDAMED last updated this device on Apr 2, 2024

92501015

843541291094

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Material clínico y sanitario, S.L
UDI-DI code: 08435412900426
Reference / catalog number: 92501015

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Manufacturer information

Organization name: Material clínico y sanitario, S.L
SRN: ES-MF-000016772
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435412900426
Basic UDI-DI: 843541291094
Reference / catalog number: 92501015
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: https://www.maclysa-sl.es/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A03020199EXTENSIONS - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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0000560B-08435412906282On the market 0000552B-08435412906299On the market 0000555B-08435412906275On the market 92501018843541291094On the market 9250103843541291094On 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.