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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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Ariel bad cabin — 2 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

Ariel bad cabin

385889357AWBC001VD

2 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: 385889357AWBC001VD
Device name: Ariel bad cabin
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 8, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KR3MKAHAP3Q9X10CA7A2X9EX

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 BC AR 200.N103858893571513
AW BC AR 100.N103858893571506