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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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Remenje za humanu imobilizaciju — 7 UDI-DI variants, MDR

MD Atlas
OTOS Ortopedska tehnika d.o.o.

Data from EUDAMED, last updated May 24, 2026

Remenje za humanu imobilizaciju

385889398970001778

7 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: OTOS Ortopedska tehnika d.o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889398970001778
Device name: Remenje za humanu imobilizaciju
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: OTOS Ortopedska tehnika d.o.o.
SRN: HR-MF-000040944
Country: Croatia
Email: otos@otos.hr
Phone: +385 31 252 000

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J9BHDBN4YH3S7M4S8CNG2ZX0

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

970002503858893981251
970002303858893981237
970002403858893981244
970002203858893981220
970001903858893981213
970001803858893981206
970001703858893981190