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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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Nima 600 Skikt Mesh — 26 UDI-DI variants, MDR (Nimacare AB)

MD Atlas
Nimacare AB

Data from EUDAMED, last updated May 31, 2026

Nima 600 Skikt Mesh

735005286600SKIKTMESH3D

26 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: Nimacare AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735005286600SKIKTMESH3D
Device name: Nima 600 Skikt Mesh
Device model: Nima 600 Skikt Mesh
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nimacare AB
SRN: SE-MF-000050989
Country: Sweden
Email: nils@nimacare.se
Phone: +46706355070

Variants by status

UDI-DI variants

26 UDI-DI variants

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Applied filters

basicUdiUlid01KS0BTCAS4CE9VCDN9D6DWZJ8

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

No registered UDI-DI variants for this device family.