Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

80 900 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

80 900 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: 04260182780909
Reference / catalog number: 80 900 00

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: TECO Medical Instruments, Production + Trading GmbH
SRN: DE-MF-000022642
Manufacturer status: Active

Related devices

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 80 920 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.

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: 04260182780909
Basic UDI-DI: 426018278CAX809Z8
Reference / catalog number: 80 900 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