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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

ALCOHOL ISO 9977/3 — IVDR Class A IVDR by Titolchimica S.p.A.

MD Atlas
Titolchimica S.p.A.

EUDAMED last updated this device on Mar 31, 2026

ALCOHOL ISO 9977/3

805005413TC45595SM

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Titolchimica S.p.A.
UDI-DI code: 08050054130101
Reference / catalog number: TC45595SS

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View device family (Basic UDI)

Manufacturer information

Organization name: Titolchimica S.p.A.
SRN: IT-MF-000028986
Manufacturer status: Active

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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.

Critical warnings

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

CW057
EUDAMED did not publish a description for this code.
CW084
EUDAMED did not publish a description for this code.
CW091
EUDAMED did not publish a description for this code.
CW139
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW999
P370+P378: In case of fire: use carbon dioxide, foam, chemical powder to estinguish

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
EL		Still on market

Device identification

Trade name: ALCOHOL ISO 9977/3
UDI-DI code: 08050054130101
Basic UDI-DI: 805005413TC45595SM
Reference / catalog number: TC45595SS
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: —
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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