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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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SinaVita® Mesh Nebulizer KS015 — 1 UDI-DI variant, MDR

MD Atlas
MIM Pharma Europe AB

Data from EUDAMED, last updated May 31, 2026

SinaVita® Mesh Nebulizer KS015

735017801073501780101456M

1 UDI-DI variant

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735017801073501780101456M
Device name: SinaVita® Mesh Nebulizer KS015
Device model: KS015
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: MIM Pharma Europe AB
SRN: SE-MF-000048118
Country: Sweden
Email: mim@mimpharma.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01K7H43ZDDGJRB7QEW12GZ4SFY

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

SV-MESH-NEB-00107350178010145