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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

42-0001459 — Class I MDR by ANTONI CARLES S.A.

MD Atlas
ANTONI CARLES S.A.

EUDAMED last updated this device on Mar 16, 2023

42-0001459

8436566193REFH6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ANTONI CARLES S.A.
UDI-DI code: 08436566195751
Reference / catalog number: 42-0001459

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Manufacturer information

Organization name: ANTONI CARLES S.A.
SRN: ES-MF-000001010
Manufacturer status: Active

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42-00000828436566191TABGEOn the market 12290948436566191TABGEOn the market 12291038436566191TABGEOn the market 42-00000808436566191TABGEOn the market 42-00000818436566191TABGEOn 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: 08436566195751
Basic UDI-DI: 8436566193REFH6
Reference / catalog number: 42-0001459
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: AC-powered device consists of a chassis block with a tabletop, a column support and a chair to facilitate support, positioning and adjustment of ophthalmic instruments, providing electronically regulated outlets and patient accommodation in a chair by means of anelectric lift group.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12120119OPHTHALMOLOGICAL TREATMENT UNITS

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

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