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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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T-Balance Plus lämpöasu — 7 UDI-DI variants, MDR (Telespro Finland Oy)

MD Atlas
Telespro Finland Oy

Data from EUDAMED, last updated May 23, 2026

T-Balance Plus lämpöasu

64298301198161UR

7 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: Telespro Finland Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64298301198161UR
Device name: T-Balance Plus lämpöasu
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2021

Manufacturer & authorised representative

Manufacturer

Name: Telespro Finland Oy
SRN: FI-MF-000011731
Country: Finland
Email: telespro@telespro.fi
Phone: +358207691250

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FPYSNWYZRH509RVE38579CSX

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

161-L/XL06429830119845
161 M06429830119838
161-S06429830119821
161-Short L/XL06429830119852
161-XS06429830119814
161-XXL06429830119869
26006429830119876