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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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Sanatyl, nesterilní — 4 UDI-DI variants, MDR (STERIWUND spol. s r.o.)

MD Atlas
STERIWUND spol. s r.o.

Data from EUDAMED, last updated May 23, 2026

Sanatyl, nesterilní

85951541042VL

4 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: STERIWUND spol. s r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85951541042VL
Device name: Sanatyl, nesterilní
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: STERIWUND spol. s r.o.
SRN: CZ-MF-000036963
Country: Czechia
Email: steriwund@steriwund.cz
Phone: +420 733 110 862

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KMJ2VY1YEDXZ2T630EHFMXKP

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

1033/3008595154115165
1033/1508595154113550
1033/6008595154115172
1033/2008595154114250