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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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ALU MB 200X45 (60-8) — 11 UDI-DI variants, MDR (Haco Tellus AB)

MD Atlas
Haco Tellus AB

Data from EUDAMED, last updated May 30, 2026

ALU MB 200X45 (60-8)

7330530DW001KJ

11 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: 7330530DW001KJ
Device name: —
Device model: ALU MB 200X45 (60-8)
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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS4NG3K7JYEMKKV72Y9HS32R

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

ALU MB 200X45 (60-8)07330530000281
HE-H PRIMO 125X33 MM SOFT07330530000472
HE-H PRIMO 146,5X37 MM07330530000564
HE-H PRIMO 146,5X37 MM USA07330530000397
HE-H PRIMO 200X28 MM USA07330530000458
HPH-E 150x27 40-8 EKERFÄLG , SVART07330530000410
HPH-E 175x27 8/53 M8-7507330530000427
HXL 100 HEL KOMPL. MED BYGEL! M1207330530000595
LÄNKHJUL HE-H PRIMO 123,5X33,5 MM07330530000465
M200007607330530006559
M500003007330530007372