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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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STÖDHJULSSATS SPECIAL 16-26 — 8 UDI-DI variants, MDR (Haco Tellus AB)

MD Atlas
Haco Tellus AB

Data from EUDAMED, last updated May 30, 2026

STÖDHJULSSATS SPECIAL 16-26

7330530AT001HU

8 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: Haco Tellus AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 7330530AT001HU
Device name: —
Device model: STÖDHJULSSATS SPECIAL 16-26
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Haco Tellus AB
SRN: SE-MF-000053610
Country: Sweden
Email: ferdo.brzica@hacotellus.se
Phone: +46732219941

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4NG31KE86NYNQ1P2HFM3X3

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

STÖDHJULS SATS FÖR CYKLAR 15007330530000168
STÖDHJULS SATS FÖR CYKLAR 20007330530000175
STÖDHJULS SATS FÖR CYKLAR 30007330530000199
STÖDHJULSSATS (GER) 16 STÖTDÄMPARE07330530000182
STÖDHJULSSATS (GER) 20 STÖTDÄMP.07330530000212
STÖDHJULSSATS (GER) 2407330530000236
STÖDHJULSSATS (GER) 28 STÖTDÄMP07330530000229
STÖDHJULSSATS SPECIAL 16-2607330530000205