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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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Tables for RAD rooms — 31 UDI-DI variants, MDR

MD Atlas
General Medical Merate S.p.A.

Data from EUDAMED, last updated May 30, 2026

Tables for RAD rooms

805489048TRDRE

31 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: General Medical Merate S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805489048TRDRE
Device name: Tables for RAD rooms
Device model: Tables for RAD rooms
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 28, 2023

Manufacturer & authorised representative

Manufacturer

Name: General Medical Merate S.p.A.
SRN: IT-MF-000023169
Country: Italy
Email: info@gmmspa.com
Phone: +39 035 45 25 311

Variants by status

UDI-DI variants

31 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HFXSZ568ZVDX4CNGVTVGBAC7

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

CT160F08054890480215
TT926208054890480857
TT922208054890480789
TT922108054890480772
BT763008054890480666
TT926108054890480840

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