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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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DOTCH® Puru® Syringes — 7 UDI-DI variants, MDR

MD Atlas
STAXS The Netherlands BV

Data from EUDAMED, last updated May 30, 2026

DOTCH® Puru® Syringes

87193273979SYS-00XX-XXE2

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: STAXS The Netherlands BV

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Device characteristics

Measuring functionAdministers medicine

Identity & classification

Basic UDI-DI: 87193273979SYS-00XX-XXE2
Device name: DOTCH® Puru® Syringes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2022

Manufacturer & authorised representative

Manufacturer

Name: STAXS The Netherlands BV
SRN: NL-MF-000005795
Country: Netherlands
Email: communication@staxs.eu
Phone: +31513677076

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FRT3W5FND3S4CBESTW0V4KYM

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

SYS-0030-2508720299269484
SYS-0005-2508719327397992
SYS-0020-2508720299269477
SYS-0001-2508719327397978
SYS-0003-2508719327397985
SYS-0050-2508720299269491
SYS-0010-2508720299269460