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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

Memo 4D Accessory tray — Class I MDR by Corcym S.r.l.

MD Atlas
Corcym S.r.l.

EUDAMED last updated this device on May 8, 2026

Memo 4D Accessory tray

8022057ACCTRAYJ8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Corcym S.r.l.
UDI-DI code: 08022057015525
Reference / catalog number: ICV1357

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View device family (Basic UDI)

Manufacturer information

Organization name: Corcym S.r.l.
SRN: IT-MF-000027865
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

G15 001664 0070Issued
Quality management systemNotified body: 0123Expiry: Nov 2, 2030
G12 001664 0050Issued
Quality management systemNotified body: 0123Expiry: Apr 3, 2028

Critical warnings

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

CW011
Consult instructions for use

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jun 1, 2021	Still on market

Device identification

Trade name: Memo 4D Accessory tray
UDI-DI code: 08022057015525
Basic UDI-DI: 8022057ACCTRAYJ8
Reference / catalog number: ICV1357
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08022057015525

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L070799CARDIAC SURGERY INSTRUMENTS, REUSABLE - 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

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