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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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Telemetry bag — 13 UDI-DI variants, MDR (Hanotex International BV)

MD Atlas
Hanotex International BV

Data from EUDAMED, last updated May 30, 2026

Telemetry bag

87193263861HITelemetryAU

13 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: Hanotex International BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87193263861HITelemetryAU
Device name: Telemetry bag
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Hanotex International BV
SRN: NL-MF-000023987
Country: Netherlands
Email: info@hanotex.nl
Phone: +31513412034

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H0FSJQ784VA961DX2TK1YDDA

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

406408719326386140
406508719326386119
406608719326386126
406708719326386133
407308719327217757
405208719326386164
405608719326386195
4052A08719326386171
405808719327217719
405708719327217702
405108719326386157
407208719327217740
406508719327217733