Organization name

Mirion Technologies (Capintec), Inc.

SRN

US-MF-000000770

Manufacturer status

Active

Primary placement in Austria; available across 32 countries total.

Trade name

Pro-Tec III, 2.5 cc

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.

00859942006584

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.

08599420061024U

Reference / catalog number

007-755

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

Syringe shields are intended to provide radiation shielding to the technician for syringes during preparation and administration of radiopharmaceuticals to patients.

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.

• Z11029099VARIOUS INSTRUMENTS FOR NUCLEAR MEDICINE - OTHER

• Class I medical devices in EUDAMED

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