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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

Y5 — Class I MDR by CORONA MEDICAL

MD Atlas
CORONA MEDICAL

EUDAMED last updated this device on Dec 20, 2023

Y5

376034596PLT5TOGUW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CORONA MEDICAL
UDI-DI code: 37603459600070
Reference / catalog number: Y5

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Manufacturer information

Organization name: CORONA MEDICAL
SRN: FR-MF-000028438
Manufacturer status: Active

Critical warnings

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

CW259
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 37603459600070
Basic UDI-DI: 376034596PLT5TOGUW
Reference / catalog number: Y5
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: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08060101HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS

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

Related devices

Ysalyde4376034596Y4UMOn the market Ysalyde 3 FE376034596YSFEK2On the market Ymagyn 4376034596YM4MHOn the market Ymagyn 3 FE376034596YMFEJ4On 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.