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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

Alkaline Phosphatase (IFCC) — IVDD — General IVDD

MD Atlas
GIESSE DIAGNOSTICS SRL

EUDAMED last updated this device on Feb 18, 2026

Alkaline Phosphatase (IFCC)

B-08053172970055

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: GIESSE DIAGNOSTICS SRL
UDI-DI code: 08053172970055
Reference / catalog number: 4183

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View device family (Basic UDI)

Manufacturer information

Organization name: GIESSE DIAGNOSTICS SRL
SRN: IT-MF-000039031
Manufacturer status: Active

Related devices

AlbuminB-08053172970024On the market AlbuminB-08053172970000On the market AlbuminB-08053172970017On the market Alkaline Phosphatase - Biotecnica SystemsB-08053172972899On the market Alkaline Phosphatase (DGKC)B-08053172972868On 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.

Critical warnings

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

CW132
EUDAMED did not publish a description for this code.
CW129
MIT - Reagente B/Reagent B

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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: Alkaline Phosphatase (IFCC)
UDI-DI code: 08053172970055
Basic UDI-DI: B-08053172970055
Reference / catalog number: 4183
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Diagnostic kit consisting of two reagents for the quantitative determination of alkaline phosphatase (ALP) in serum and plasma with a method optimized according to IFCC.
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.

W01010105ALKALINE PHOSPHATASE - TOTAL

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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