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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

80 920 00 — IVDR Class A IVDR by TECO Medical…

MD Atlas
TECO Medical Instruments, Production + Trading GmbH

EUDAMED last updated this device on Feb 2, 2023

80 920 00

426018278CAX809Z8

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: TECO Medical Instruments, Production + Trading GmbH
UDI-DI code: 04260182780954
Reference / catalog number: 80 920 00

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Manufacturer information

Organization name: TECO Medical Instruments, Production + Trading GmbH
SRN: DE-MF-000022642
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: 04260182780954
Basic UDI-DI: 426018278CAX809Z8
Reference / catalog number: 80 920 00
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: user manual, safety information
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0202020102AUTOMATED COAGULOMETERS

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

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85001 / 81 102 10426018278CMX81152On the market 85002 / 81 102 20426018278CMX81152On the market 85004 / 81 102 40426018278CMX81152On the market D2020-005B-DD-D2020-0057EOn the market 80 900 00426018278CAX809Z8On 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.