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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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THOLOMEUS — 1 UDI-DI variant, MDR (Biotechmed S.r.l.)

MD Atlas
Biotechmed S.r.l.

Data from EUDAMED, last updated May 30, 2026

THOLOMEUS

805969359THOLOMEUSJ7

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Biotechmed S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805969359THOLOMEUSJ7
Device name: THOLOMEUS
Device model: Version 2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Dec 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: Biotechmed S.r.l.
SRN: IT-MF-000030231
Country: Italy
Email: info@biotechmed.it
Phone: +39 0331 982129

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01JEXF2KJ6YJ9XVG8VZFB41RW1

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

Version 2.6.008059693592608