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EUDAMED last updated this device on Jun 30, 2026
764015897GERDOFFPLUSCNESOXX REFLUX DEFENCE is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by SOFAR SWISS SA. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
07640158970713ERD-C04L(01)07640158970713
European Medical Device Nomenclature — the EU product classification assigned to this device.
G99GASTROINTESTINAL DEVICES - OTHER1 warning recorded — scroll inside the panel to see all entries.
OTHER
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
CH-MF-000047475CSQ0028250925CVD0045250125The 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.
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 →764015897GERDOFFSEOn the marketESOXX DEFENCE764015897GERDOFFSEOn the marketESOXX DEFENCE764015897GERDOFFSEOn the marketESOXX REFLUX DEFENCE764015897GERDOFFPLUSCNOn the marketESOXX REFLUX PROTECTIONB-07640158970645On the marketESOXX REFLUX PROTECTION & ACID DEFENCE764015897GERDOFFSEOn the marketCertificate health across this manufacturer's portfolio.
CVD0045250125SupplementedNotified 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.
CSQ0028250925SupplementedNotified 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.
CVD0043250725SupplementedNotified 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.