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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

0.01.0002 — IVDR Class A IVDR by Axel Löser Messtechnik

MD Atlas
Axel Löser Messtechnik

EUDAMED last updated this device on May 18, 2022

0.01.0002

PP12562CALLOESUNG20

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Axel Löser Messtechnik
UDI-DI code: 13125620.01.0002028
Reference / catalog number: 0.01.0002

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Manufacturer information

Organization name: Axel Löser Messtechnik
SRN: DE-MF-000023401
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 13125620.01.0002028
Basic UDI-DI: PP12562CALLOESUNG20
Reference / catalog number: 0.01.0002
Issuing entity: IFA

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.

EMDN nomenclature code(s)

W0101050303AQUEOUS STANDARDS (CC)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

0.01.0001PP12562CALLOESUNG20On the market TYP16.CPP12562OSMOMETER42On the market TYP7iMPP12562OSMOMETER42On the market TYP7PP12562OSMOMETER42On the market TYP16MPP12562OSMOMETER42On 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.