Organization name

France Chirurgie Instrumentation SAS

SRN

FR-MF-000000463

Manufacturer status

Active

6 warnings recorded — scroll inside the panel to see all entries.

• Consult instructions for use
• Defibrillation-proof type B applied part
• Do not re-use
• Do not resterilize
• Do not use if package is damaged
• Caution

  See product instruction for use

Primary placement in France; available across 13 countries total.

Trade name

Ciliprobe™ – IRIDEX

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.

23700773724424

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.

3700773707329L

Reference / catalog number

S9.1701

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

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• Q02040302OCULAR CYCLOPHOTOCOAGULATION FIBERS, SINGLE-USE

• Class I medical devices in EUDAMED

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