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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

ISO.5000 — IVDR Class A IVDR by Micras di Cipressi…

MD Atlas
Micras di Cipressi Gabriele

EUDAMED last updated this device on Jan 6, 2025

ISO.5000

805772495SOLVP8

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Micras di Cipressi Gabriele
UDI-DI code: 08057724951783
Reference / catalog number: ISO.5000

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View device family (Basic UDI)

Manufacturer information

Organization name: Micras di Cipressi Gabriele
SRN: IT-MF-000044290
Manufacturer status: Active

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW058
EUDAMED did not publish a description for this code.
CW077
EUDAMED did not publish a description for this code.
CW107
EUDAMED did not publish a description for this code.
CW117
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08057724951783
Basic UDI-DI: 805772495SOLVP8
Reference / catalog number: ISO.5000
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Isoparaffin based solvent for histology and cytology - 5 l
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

EMDN nomenclature code(s)

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

W01030799HISTOLOGY / CYTOLOGY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

KAB1.30805772495CARBGUOn the market KAB.30805772495CARBGUOn the market KABP.30805772495CARBGUOn the market SL100.2500 805772495SOLVP8On the market SL100.5000805772495SOLVP8On 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.