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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

TYP16.CM — IVDR Class A IVDR by Axel Löser Messtechnik

MD Atlas
Axel Löser Messtechnik

EUDAMED last updated this device on May 18, 2022

TYP16.CM

PP12562OSMOMETER42

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: 1312562TYP16.CM091
Reference / catalog number: TYP16.CM

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Manufacturer information

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

Related devices

0.01.0001PP12562CALLOESUNG20On the market 0.01.0002PP12562CALLOESUNG20On the market TYP16.CPP12562OSMOMETER42On the market TYP7iMPP12562OSMOMETER42On the market TYP7PP12562OSMOMETER42On the market

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: 1312562TYP16.CM091
Basic UDI-DI: PP12562OSMOMETER42
Reference / catalog number: TYP16.CM
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)

W0299IVD INSTRUMENTS - OTHER

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

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.