Organization name

SURGIRIS

SRN

FR-MF-000004556

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• See user manual before use

  OTHER

Primary placement in France; available across 31 countries total.

Trade name

X3MT

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.

03701502626497

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.

37015026000138

Reference / catalog number

CX3CF/T

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

X3MT SINGLE YOKE

Additional information URL

https://www.surgiris.com/

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.

• Z12010701FIXED SCIALYTIC LAMPS

• Class I medical devices in EUDAMED

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