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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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Tamla Knee Splint — 3 UDI-DI variants, MDR (Pedihealth Oy)

MD Atlas
Pedihealth Oy

Data from EUDAMED, last updated May 23, 2026

Tamla Knee Splint

64300715315638TC9

3 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: Pedihealth Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64300715315638TC9
Device name: Tamla Knee Splint
Device model: Tamla Knee Splint
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 25, 2021

Manufacturer & authorised representative

Manufacturer

Name: Pedihealth Oy
SRN: FI-MF-000000503
Country: Finland
Email: info@pedihealth.fi
Phone: + 358 207401330

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FNB72EYRNRQS1RXZZJ8NDZZ9

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

Tamla Knee Splint L06430071530085
Tamla Knee Splint M06430071530078
Tamla Knee Splint S06430071530061