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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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Tinearity — 4 UDI-DI variants, MDR (Circius Pharma AB)

MD Atlas
Circius Pharma AB

Data from EUDAMED, last updated May 31, 2026

Tinearity

735013396Tinearity1Z5

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Circius Pharma AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735013396Tinearity1Z5
Device name: Tinearity
Device model: G1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Circius Pharma AB
SRN: SE-MF-000013023
Country: Sweden
Email: info@circiuspharma.com
Phone: +46 31 818400

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVYKFHDZXR3GMXM90S34QWTB

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

600107350133961024
600007350133961000
600607350133961109
604207350133961123