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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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GAMMAPRO — 3 UDI-DI variants, MDR

MD Atlas
GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.

Data from EUDAMED, last updated May 23, 2026

GAMMAPRO

8437018413GAMMAPROBE7U

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.

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Device characteristics

Active deviceReusableMeasuring function

Identity & classification

Basic UDI-DI: 8437018413GAMMAPROBE7U
Device name: GAMMAPRO
Device model: STD, LAP, HI-S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: GENERAL EQUIPMENT FOR MEDICAL IMAGING, S.A.
SRN: ES-MF-000013779
Country: Spain
Email: calidad@oncovision.com
Phone: +34 963722472

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FNRDFNPSMZBK0MYTZXSMQB5A

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

GAMMAPRO HI-S08437018413096
GAMMAPRO LAP08437018413089
GAMMAPRO STD08437018413072