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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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Synchro REV — 1 UDI-DI variant, MDR (Technogym spa)

MD Atlas
Technogym spa

Data from EUDAMED, last updated May 30, 2026

Synchro REV

805071466DFHM3A08M

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Technogym spa

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805071466DFHM3A08M
Device name: Synchro REV
Device model: DFHM3A0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: Technogym spa
SRN: IT-MF-000009974
Country: Italy
Email: prrc@technogym.com
Phone: +393427489099

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01HV9H40EDZEFPMPQVYPM14TDX

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

DFHM3A008050714660665