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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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Electrical Bad — 9 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

Electrical Bad

385889357AWHC001XF

9 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: 385889357AWHC001XF
Device name: —
Device model: Electrical Bad
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

9 UDI-DI variants

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Applied filters

basicUdiUlid01KR0WWMSCFWDP5RH5MN2VBTXY

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 HC CB 00303858893571452
AW HC DB 00303858893571490
AW HC CB 00103858893571438
AW HC SUB 00103858893571414
AW HC DB 00103858893571476
AW HC BB 00103858893571421
AW HC CB 00203858893571445
AW HC CB 00403858893571469
AW HC DB 00203858893571483