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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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TQURA — 561 UDI-DI variants, MDR (OPTIMA MOLLITER SRL)

MD Atlas
OPTIMA MOLLITER SRL

Data from EUDAMED, last updated May 31, 2026

TQURA

805715830-TQURA-FS

561 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: OPTIMA MOLLITER SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805715830-TQURA-FS
Device name: TQURA
Device model: TQURA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: OPTIMA MOLLITER SRL
SRN: IT-MF-000022195
Country: Italy
Email: info@optimamolliter.com
Phone: +390733801060

Variants by status

UDI-DI variants

561 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBZZB041HPKR553A9HFSTB11

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

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C1D-ROSEECO LEATHER STR.PHARD3608057158305367
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C1Y-TAOTES CBBK4108054794787281
C1Y-TAOTES CBGY3808054794787823
C1Y-TORITESSUTOBLUE NAVY3908052211761258
C1Y-UKETESSUTOBLACK4108052211762606
C1Y-NOAHKNITTED STRETCHBLACK3908054794780039