- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Dec 2, 2025
37004836Spatulas1NJCuller Iris Spatulas. very delicate. 1 mm 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.
FR-MF-000000336(01)03700483607846
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 1 country total.
Placed on the market in France; per-country availability dates not published.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03700483607846Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
37004836Spatulas1NJ9611BUDI 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.
L1706OPHTHALMOLOGY SPATULAS, 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 →37004836Forceps1C2On the marketCrozafon-De-Laage Punch. semicircular cut37004836Punch1ADOn the marketCulbertson Marker37004836Markers1BTOn the marketCURVED BLADE ADJUSTABLE SPECULUM37004836Speculums1WXOn the marketDBLE-ENDED SEIBEL NUCLEUS CHOPPER, RIGHT37004836HooksYROn the marketDe Laage Glaucoma Forceps37004836Forceps1C2On 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.