- Role
- Country
- Date of registration
- Address
CN-MF-000047100No 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.Sperm Mitochondrial Membrane Potential Staining Kit (JC-1, Flow Cytometry)（20 tests/kit） is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Chengdu Legend-Tec Technology Co.,Ltd. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 22, 2026
697735700202M4Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)06977357002022
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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.
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.
Primary placement in Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
06977357002022Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
697735700202M4202UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02020499FLOW CYTOMETRY INSTRUMENTS - OTHER697735700206MCOn the marketSperm DNA Fragmentation Assay Kit（Flow Cytometry）(20 tests/kit)697735700200LYOn the marketSperm DNA Fragmentation Assay Kit（Flow Cytometry）（50 tests/kit）697735700200LYOn the marketSperm Mitochondrial Membrane Potential Staining Kit (JC-1, Flow Cytometry)（50 tests/kit）697735700202M4On the marketSperm ROS Staining Kit (Flow Cytometry)（20 tests/kit）697735700204M8On the marketSperm ROS Staining Kit (Flow Cytometry)（50 tests/kit）697735700204M8On the marketNo certificate specifically references this device's Basic UDI-DI.