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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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Suture Passer System — 9 UDI-DI variants, MDR (RZ-Medizintechnik GmbH)

MD Atlas
RZ-Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Suture Passer System

40491975225-820-SPSQW

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RZ-Medizintechnik GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40491975225-820-SPSQW
Device name: Suture Passer System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: RZ-Medizintechnik GmbH
SRN: DE-MF-000005616
Country: Germany
Email: info@rz-medizintechnik.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GR0WQZ5RSZVQ8H5B4E2MPSYW

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

Suture Passer04049197521635
Suture Passer04049197521611
Suture Passer04049197521642
Suture Passer04049197505550
Suture Passer04049197519168
Suture Passer04049197519113
Suture Passer04049197521628
Suture Passer Needle04049197506977
Suture Passer Needle steril04049197518734