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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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Crosstape — 5 UDI-DI variants, MDR (True Tape Sports GmbH)

MD Atlas
True Tape Sports GmbH

Data from EUDAMED, last updated May 23, 2026

Crosstape

PP0944214047

5 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: True Tape Sports GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP0944214047
Device name: Crosstape
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: True Tape Sports GmbH
SRN: DE-MF-000036380
Country: Germany
Email: info@truetape.de

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JJQ0M79EZMXJZ3E9X0SXRNK3

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

1404111970655394
1402111673128932
1405111965680303
1406111937494443
1403111978852228