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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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Hercul — 5 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

Hercul

385889357AWPL00149

5 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: 385889357AWPL00149
Device name: Hercul
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KRG8YGM21RWQC25H1WP62FNK

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 PL ST 01.00703858893571308
AW PL AL 05.00703858893574699
AW PL ST 04.00703858893574682
AW PL ST 02.00703858893571315
AW PL ST 03.00703858893574675