Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Turbocast — 47 UDI-DI variants, MDR (Ttape Company)

MD Atlas
Ttape Company

Data from EUDAMED, last updated May 31, 2026

Turbocast

871797315LTTP-001OTGQ

47 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 871797315LTTP-001OTGQ
Device name: Turbocast
Device model: LTTP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 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

47 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KQVKQ00VNE8S77RB4P78EK64

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

161108717973150176
250208717973150459
250308717973150473
Turbocast08717973150206
080308717973150046
201008717973150268
2502/908717973150466
203008717973150367
200408717973150251
200208717973150237
080408717973150053
202008717973150312
080208717973150039
250008717973150411
161208717973150183
200308717973150244
2501/908717973150442
201108717973150275
080108717973150022
081108717973150077
200008717973150213
161008717973150169
203308717973150398
160008717973150114
203108717973150374

1 2