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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

AL700003 — IVDR Class A IVDR by Technogenetics S.p.A

MD Atlas
Technogenetics S.p.A

EUDAMED last updated this device on Oct 26, 2022

AL700003

805432095AL1200TRIGGERLA

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Technogenetics S.p.A
UDI-DI code: 08054320951001
Reference / catalog number: AL700003

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Manufacturer information

Organization name: Technogenetics S.p.A
SRN: IT-MF-000025331
Manufacturer status: Active

Critical warnings

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

CW265
Solution containing sodium hydroxide C ≤ 2%.
CW011
The AL1200 Trigger set is for in vitro diagnostic use only and is not for internal use in humans or animals. Technogenetics will not be held responsible for any loss or damage (except as required by statute) howsoever caused, arising out of non-compliance with the instructions provided.

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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: 08054320951001
Basic UDI-DI: 805432095AL1200TRIGGERLA
Reference / catalog number: AL700003
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: 2
Additional product description: Trigger Set is an in vitro diagnostic device intended to be used on the automated AL1200 analyzer. Trigger Set contains two different Solutions (Trigger A and Trigger B) for generating luminescent signal in the AL1200 Analyzer 120.The Trigger Set is used in conjunction with AL1200 chemiluminescent immunoassay reagents.
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.

W01029099IMMUNOCHEMISTRY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.