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EUDAMED last updated this device on Mar 16, 2026
6973315739290B4Vazyme Comprehensive Exome Dx Panel is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Nanjing Vazyme Medical Technology Co.,Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06973315739290NC001ME-01(01)06973315739290
European Medical Device Nomenclature — the EU product classification assigned to this device.
W010699GENETIC TESTS - OTHERCN-MF-000031032The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Spain; available across 1 country total.
Placed on the market in Spain; per-country availability dates not published.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
EU-TDA-FI-66922-800033-2025IssuedEU-QMS-FI-01219-800033-2025IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →6973315739399BTOn the marketVAMNE MagUltra Circulating Cell-free DNA Isolation Mini Kit6973315736367AROn the marketVAMNE MaqUltra Circulating Cell-free DNA lsolation Mini Kit (Prepackaged)VAMNE MagUltra Circulating Cell-free DNA Isolation Mini Kit (Prepackaged)6973315736367AROn the marketVazyme MedExome Dx Panel6973315739337B5On the marketVazyme Precision CS18 Dx Panel6979469760333M7On the marketVazyme Precision PN30 Dx Panel6979469760340M4On the marketNo certificate specifically references this device's Basic UDI-DI.