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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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Minisart® HY | SRP — 2 UDI-DI variants, MDR

MD Atlas
Sartorius Stedim Biotech GmbH

Data from EUDAMED, last updated May 23, 2026

Minisart® HY | SRP

4063233MIPTFE020MBSNCNSRT

2 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: Sartorius Stedim Biotech GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4063233MIPTFE020MBSNCNSRT
Device name: Minisart® HY | SRP
Device model: Minisart® HY | SRP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jun 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Sartorius Stedim Biotech GmbH
SRN: DE-MF-000017607
Country: Germany
Email: prrc-st@sartorius.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JYG9WVM83DFMY3KTXPSDNXW8

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

16596--------HYQ04063233000724
16599--------HYQ04063233000731