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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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MOBILIS ColluActive 2 w 1 Kołnierz… — 12 UDI-DI variants, MDR

MD Atlas
SIGVARIS SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

MOBILIS ColluActive 2 w 1 Kołnierz szyjny półsztywny

5906699ColluActive2w178

12 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: SIGVARIS SPÓŁKA AKCYJNA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5906699ColluActive2w178
Device name: —
Device model: MOBILIS ColluActive 2 w 1 Kołnierz szyjny półsztywny
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: SIGVARIS SPÓŁKA AKCYJNA
SRN: PL-MF-000004824
Country: Poland
Email: sekretariat@sigvaris.com
Phone: +48 61 43 88 200

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01KRBGFZRKPQEFDX2BQFF7CC5N

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

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35954305906699077789
35955005906699077857
35954205906699077772
35954105906699077765
35954505906699077802
35954905906699077840
35954805906699077833
35954405906699077796
35955105906699077864
35955205906699077871
35954605906699077819