Organization name

Medical Innovation Design MID AB

SRN

SE-MF-000053189

Manufacturer status

Active

Primary placement in Sweden; available across 12 countries total.

Trade name

Hakon Carbon Detector Shield

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.

07350132810224

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.

73501328DH23-01SQ

Reference / catalog number

24

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

Hakon Carbon Detectorshield Item No. DH23-01 Molded Adapted for Siemens detectors for Mobilett Elara, Ysio MAX and Multitom RAX.

Additional information URL

https://www.mid.nu/produkter/hakon-carbon-detectorshield-artnr-dh23-01

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.

• Z11030580RADIOLOGY INSTRUMENTS - HARDWARE ACCESSORIES

• Class I medical devices in EUDAMED

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