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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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S cast — 2 UDI-DI variants, MDR (Ttape Company)

MD Atlas
Ttape Company

Data from EUDAMED, last updated May 31, 2026

S cast

871797315LTTP-007OTHN

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: Ttape Company

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871797315LTTP-007OTHN
Device name: S cast
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ttape Company
SRN: NL-MF-000003944
Country: Netherlands
Email: d.jacobs@turbocast.eu
Phone: +32496590396

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KSJ2SJHG3YY4MB9YY72JA7SV

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

S-CAST - 60X44CM X 1,6MM - NON PERFO - LIGHT BEIGE08717973152743
Scast08717973152736