- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 11, 2026
37011602PTEA000296Surgical instruments for isa™ total and partial shoulder prosthesis is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MOVE-UP. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
FR-MF-000000412(01)03701160202521
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.
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 placement in France; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Mar 13, 2019 | Still on market |
| EL | Oct 22, 2025 | Still on market |
| Spain | Feb 2, 2022 | Still on market |
| Italy | Aug 1, 2023 | 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.
03701160202521Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
37011602PTEA0002960105A0000UDI 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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L091102ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLEPrimary 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.
MDR 723851SupplementedNotified 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 →37011602PTEA000398On the marketSurgical instruments for isa™ total and partial shoulder prosthesis37011602PTEA000398On the marketSurgical instruments for isa™ total and partial shoulder prosthesis37011602PTEA000398On the marketSurgical instruments for isa™ total and partial shoulder prosthesis37011602PTEA000398On the marketSurgical instruments for isa™ total and partial shoulder prosthesis37011602PTEA000398On the marketSurgical instruments for isa™ total and partial shoulder prosthesis37011602PTEA000398On the marketNo certificate specifically references this device's Basic UDI-DI.