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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

OR-1166011 — IVDR Class A IVDR by DAS Srl

MD Atlas
DAS Srl

EUDAMED last updated this device on May 19, 2026

OR-1166011

805961666APIFABLOTLE

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DAS Srl
UDI-DI code: 08059616660049
Reference / catalog number: OR-1166011

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View device family (Basic UDI)

Manufacturer information

Organization name: DAS Srl
SRN: IT-MF-000035583
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Mar 27, 2014	Still on market
Italy	Apr 7, 2015	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08059616660049
Basic UDI-DI: 805961666APIFABLOTLE
Reference / catalog number: OR-1166011
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

UDI-DI DataMatrix

Encoded

(01)08059616660049

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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.

W0201020102AUTOMATED IMMUNOCHEMISTRY ANALYSERS - MODERATE ROUTINE (Throughput > 100 and <= 250 test/h)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

OR-1013112805961666APBLOTLAOn the market OR-101600805961666APIFAG9On the market OR-102401805961666APELISATZOn the market OR-102403805961666APELISAIFABLOTMAOn the market OR-102402805961666APELISAIFAG2On 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.