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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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Nil Medical Pump Holder — 5 UDI-DI variants, MDR (Nil Medical AB)

MD Atlas
Nil Medical AB

Data from EUDAMED, last updated May 31, 2026

Nil Medical Pump Holder

7350171470029M

5 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: Nil Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7350171470029M
Device name: Nil Medical Pump Holder
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nil Medical AB
SRN: SE-MF-000051068
Country: Sweden
Email: info@nilmedical.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KS9YQGHWJVAAZYMZ226DH24M

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

N200507350171470304
N200307350171470151
N200207350171470144
N200107350171470137
N200407350171470168