Organization name

Moria S.A.

SRN

FR-MF-000000336

Manufacturer status

Active

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Trade name

Art. Chamber for Single-Use Trephine

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

03700483608973

Basic UDI-DI

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.

37004836Art-chambers23P

Reference / catalog number

17204

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

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.

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Single use instrument for ophthalmic surgery

Additional information URL

https://www.moria-surgical.com/resources-center?types[0]=3&page=1&limit=12&_=1761730662608

Clinical sizes

No clinical sizes registered for this device.

1 packaging level registered — each level carries its own UDI-DI.

• 03700483608973× 1 unitBase unit
  • 03700483603367× 1 unit

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Q020299CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHER

• Class I medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

No certificate specifically references this device's Basic UDI-DI.