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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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Ikki 100 — 10 UDI-DI variants, MDR (Awatar Medical Aid d.o.o.)

MD Atlas
Awatar Medical Aid d.o.o.

Data from EUDAMED, last updated May 24, 2026

Ikki 100

385889357AWR001S9

10 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: Awatar Medical Aid d.o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889357AWR001S9
Device name: Ikki 100
Device model: Ikki
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Awatar Medical Aid d.o.o.
SRN: HR-MF-000025777
Country: Croatia
Email: info@awatar.hr

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KR0RBJCA6NG7B6P9CS57WC8X

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

AW RFAL4W X2.00303858893570837
AW RFAL4W X3.00303858893570844
AW RST4W X2.00503858893570950
AW RAL4W X2.00703858893570875
AW RAL4W X6.00503858893570912
AW RAL4W X4.00703858893570899
AW RFAL4W X1.00703858893570820
AW RAL4W X1.00203858893570868
WAW RST3W X1.00603858893570936
AW RAL4W X7.00703858893570929