- Organization name
- UDI-DI code
- Reference / catalog number
CA-MF-000024015FOLDABLE & ADJUSTABLE THORACIC SUPPORT HARDWARE (FIXED ON BACKPOST) - LEFT is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Les Equipements Adaptés PHYSIPRO INC. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Aug 12, 2026
++G094PHYBACKRESTNVPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
+G094D5575G0Z
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
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 7 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
| Belgium | — | Still on market |
| Germany | — | Still on market |
| Spain | — | Still on market |
| Italy | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | 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.
+G094D5575G0ZBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++G094PHYBACKRESTNVD5575GUDI 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.
Y180980SEATING SYSTEMS / POSTURE SYSTEMS / SEATING AIDS - ACCESSORIES++G094PHYHEADRESTSP2On the marketFLAT AMPUTEE SUPPORT CUSHION - 7" X 8" X 2" (17 X 20 X 5 CM)++G094PHYLOWERLIMBSDNOn the marketFLAT AMPUTEE SUPPORT CUSHION - 8" X 11" X 2" (20 X 28 X 5 CM)++G094PHYLOWERLIMBSDNOn the marketFOLDABLE & ADJUSTABLE THORACIC SUPPORT HARDWARE (FIXED ON BACKPOST) - RIGHT++G094PHYBACKRESTNVOn the marketFOLDABLE & ADJUSTABLE THORACIC SUPPORT HARDWARE (KIT HP2) - LEFT++G094PHYBACKRESTNVOn the marketFOLDABLE & ADJUSTABLE THORACIC SUPPORT HARDWARE (KIT HP2) - RIGHT++G094PHYBACKRESTNVOn the marketNo 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.