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FR-MF-000000336OU LC Guide Ring for Artificial Chamber 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.
EUDAMED last updated this device on Oct 29, 2025
37004836Art-chambers23PPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03700483603428
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.
03700483603428Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
37004836Art-chambers23P19186UDI 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.
1 packaging level registered — each level carries its own UDI-DI.
03700483603428× 1 unitBase unit03700483603435× 5 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
Q020299CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Certificate 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.
View in glossary →B-03700483603404On the marketOU LC 500 Head-Art. ChamberB-03700483603947On the marketOU LC 550 Head-Art. ChamberB-03700483603961On the marketOU LC RING FOR ALTK ARTIFICIAL CHAMBER37004836Art-chambers13MOn the marketOUP HANDPIECE F/ ARTIFCIAL CHAMBERB-03700483609918On the marketOUP LC -1 REUSABLE SUCTION RINGB-03700483609017On the market