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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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FOTHÅLLARE XL 286X141/108 — 4 UDI-DI variants, MDR (Haco Tellus AB)

MD Atlas
Haco Tellus AB

Data from EUDAMED, last updated May 31, 2026

FOTHÅLLARE XL 286X141/108

7330530FR001K5

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: Haco Tellus AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 7330530FR001K5
Device name: —
Device model: FOTHÅLLARE XL 286X141/108
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4NHSVX0JR6M0W3Y88J0HTQ

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

FOTHÅLLARE L 236X115/8907330530002933
FOTHÅLLARE M 209X103/7307330530002926
FOTHÅLLARE XL 286X141/10807330530002940
FOTHÅLLARE XXL 329X158/12507330530002957