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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 Plan Kupad — 7 UDI-DI variants, MDR (Nimacare AB)

MD Atlas
Nimacare AB

Data from EUDAMED, last updated May 31, 2026

Nima Plan Kupad

735005286NPKJG

7 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: 735005286NPKJG
Device name: Nima Plan Kupad
Device model: Nima Plan Kupad
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KS17GPCHBZV5NESSWDJW4Y3S

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

Nima Plan Kupad 35x35 cm07333376018878
Nima Plan Kupad 40x40 cm07333376018885
Nima Plan Kupad 40x45 cm07333376018892
Nima Plan Kupad 45x40 cm07333376018908
Nima Plan Kupad 45x45 cm07350052868664
Nima Plan Kupad 50x45 cm07333376018915
Nima Plan Kupad 50x50 cm07333376018922