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EUDAMED last updated this device on May 20, 2026
697144961ECTSHMedical Cable Assemblies is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Shenzhen Envisen Industry Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06971449611734XT-9093-5001 packaging level registered — each level carries its own UDI-DI.
06971449611734× 1 unitBase unit16971449611731× 130 units(01)06971449611734
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1203020299MULTI–PARAMETER MONITORS - OTHER1 warning recorded — scroll inside the panel to see all entries.
1. The extension cable must be used in connection with specific equipment and sensor only .The user shall be responsible for ensuring extension cable compatibility with the monitoring device and sensor by referring to the Instructions For Use. The extension cable must be used by trained clinical professionals, otherwise product performance may be compromised or personal injury may occur. 2. Stop usage immediately if the cable is found to be damaged, contaminated or is showing signs of aging. 3. Do not pull or bend the cable. Improper use may cause damage to internal wires. 4. Disposal of used or expired products must be in accordance with applicable hospital regulations or local laws to avoid environmental pollution.
CN-MF-000010838The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Germany; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Aug 15, 2009 | Still on market |
| Denmark | Mar 22, 2022 | Still on market |
| Finland | Mar 13, 2023 | Still on market |
| Norway | Mar 12, 2021 | Still on market |
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 →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
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 →697144961HPDT7On the marketHead Positioning Device697144961HPDT7On the marketHead Positioning Device697144961HPDT7On the marketMedical Cable Assemblies697144961ECTSHOn the marketMedical Cable Assemblies697144961ECTSHOn the marketMedical Cable Assemblies697144961ECTSHOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
HZ 2094002-1IssuedNotified 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 →