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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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TRIAL FRAME — 2 UDI-DI variants, MDR (CI.O.M. srl)

MD Atlas
CI.O.M. srl

Data from EUDAMED, last updated May 30, 2026

TRIAL FRAME

803386634TFVJ

2 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: CI.O.M. srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803386634TFVJ
Device name: TRIAL FRAME
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2022

Manufacturer & authorised representative

Manufacturer

Name: CI.O.M. srl
SRN: IT-MF-000013093
Country: Italy
Email: info@ciom.it
Phone: +39 2 33402669

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FSSEWZ686HMHAMGNR3J14J9J

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

120/T UNIVERSAL TRIAL FRAME08033866340203
122/TN08033866340210