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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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Klavikulární bandáž 070A — 4 UDI-DI variants, MDR (HANDICAP, a.s.)

MD Atlas
HANDICAP, a.s.

Data from EUDAMED, last updated May 23, 2026

Klavikulární bandáž 070A

859404276001J7

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: HANDICAP, a.s.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859404276001J7
Device name: Klavikulární bandáž 070A
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: HANDICAP, a.s.
SRN: CZ-MF-000001007
Country: Czechia
Email: info@handicap.as

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRG3ZG2M0WP586G80YB0SN63

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

070A08594042764775
070A08594042764782
070A08594042764928
070A08594042764768