- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED data as of Jun 25, 2026
EUDAMED last updated this device on Apr 13, 2026
7290018434INS83AL Motor mount Click Driver short is an EU MDR-regulated medical device on the European market. It is classified as Class I. Manufactured by MSDI Medical Systems and Devices International Ltd.. Placed on the EU market in France. Explore certificates, regulatory status and the official record on MD Atlas.
07290018435816MCDS(01)07290018435816
European Medical Device Nomenclature — the EU product classification assigned to this device.
P01020180DENTAL IMPLANTS - ACCESSORIES1 warning recorded — scroll inside the panel to see all entries.
IL-MF-000033949The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Mar 31, 2020 | Apr 14, 2026 |
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
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.
UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
No certificate specifically references this device's Basic UDI-DI.
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.7290018434INS83On the marketAL Implant Hand Driver Short7290018434INS83On the marketAL Motor mount Click Driver long7290018434INS83On the marketAL Ratchet Click Driver Long7290018434INS83On the marketAL Ratchet Click Driver Short7290018434INS83On the marketAL Ratchet Click Driver Short 7mm7290018434INS83On the market