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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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Catheter Tray 1000mm — 6 UDI-DI variants, MDR (Stille AB)

MD Atlas
Stille AB

Data from EUDAMED, last updated May 31, 2026

Catheter Tray 1000mm

73323395004PB

6 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: Stille AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73323395004PB
Device name: Catheter Tray 1000mm
Device model: 555-1750
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Stille AB
SRN: SE-MF-000001228
Country: Sweden
Email: katalin.daroczy@stille.se
Phone: +46 72 402 34 14

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JT0VKF4MGETEH0TPNGFWREW6

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

505-113107332339227029
555-175107332339242442
555-175007332339242435
535-175007332339220754
535-175107332339220761
535-175207332339220778