- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Dec 2, 2025
37004836Spatulas1NJKoch Spatula is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Moria S.A.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03700483610860M0712(01)03700483610860
European Medical Device Nomenclature — the EU product classification assigned to this device.
L1706OPHTHALMOLOGY SPATULAS, REUSABLEFR-MF-000000336The 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.
Placed on the market in France; per-country availability dates not published.
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 →No certificate specifically references this device's Basic UDI-DI.
37004836Forceps1C2On the marketKelman-McPherson Forceps short37004836Forceps1C2On the marketKOCH MARKER FOR 5.5MM RHEXIS37004836Markers1BTOn the marketKOCH SPATULA37004836Forceps2C4On the marketKraff-Moria Forceps ergonomic oblique teeth 0.1mm tying platforms37004836Forceps1C2On the marketKratz Cannula capsule, opening 27 G. diameter 0.6 mm37004836Cannulas16LOn the marketCertificate health across this manufacturer's portfolio.
39713SupplementedNotified 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.
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