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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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TELERIA — 6 UDI-DI variants, MDR (Mediberg S.r.l. Unipersonale)

MD Atlas
Mediberg S.r.l. Unipersonale

Data from EUDAMED, last updated May 31, 2026

TELERIA

8030413FTN02MY

6 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: Mediberg S.r.l. Unipersonale

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8030413FTN02MY
Device name: TELERIA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Mediberg S.r.l. Unipersonale
SRN: IT-MF-000012712
Country: Italy
Email: info@mediberg.com
Phone: +39 035 83 54 911

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K6G7B31XZY06DWC2QN7PDJDC

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

301073GA2NME08030413319590
106049CB2NME08030413306620
105325BC2NME08030413312287
105325EE2NME08030413304770
105325AH2NME08030413312263
300140BA2NME08030413091526