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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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Transpara — 3 UDI-DI variants, MDR (ScreenPoint Medical)

MD Atlas
ScreenPoint Medical

Data from EUDAMED, last updated May 30, 2026

Transpara

8720387058Transpara_V2D5

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: ScreenPoint Medical

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720387058Transpara_V2D5
Device name: Transpara
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: ScreenPoint Medical
SRN: NL-MF-000000241
Country: Netherlands
Email: info@screenpointmed.com
Phone: +31 242020020

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HFEF609V7E20AZQ0YTW8YNBZ

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

Transpara08720387058068
Transpara08720387058044
Transpara08720387058051