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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

TE1081 — IVDD — General IVDD by TECOmedical AG

MD Atlas
TECOmedical AG

EUDAMED last updated this device on Dec 27, 2024

TE1081

B-07640146270146

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: TECOmedical AG
UDI-DI code: 07640146270146
Reference / catalog number: TE1081

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Manufacturer information

Organization name: TECOmedical AG
SRN: CH-MF-000030341
Manufacturer status: Active

Related devices

TE1017-2B-07640146270047On the market TE1067B-07640146270078On the market TE1013B-07640146270023On the market TE1012B-07640146270016On the market TE1069B-07640146270108On 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.

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: 07640146270146
Basic UDI-DI: B-07640146270146
Reference / catalog number: TE1081
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: Qualitative measurement of Candida Mannan antigen in human serum samples.
Additional information URL: https://www.tecomedical.com/login
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0105060302CANDIDA ALBICANS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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