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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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Oxisept — 2 UDI-DI variants, MDR (ЖИВАС ООД)

MD Atlas
ЖИВАС ООД

Data from EUDAMED, last updated May 23, 2026

Oxisept

3800228240134W

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: ЖИВАС ООД

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2025-MDR/QS-043
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Aug 15, 2025 → Aug 15, 2028

Identity & classification

Basic UDI-DI: 3800228240134W
Device name: Oxisept
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: ЖИВАС ООД
SRN: BG-MF-000019745
Country: Bulgaria
Email: zhivas@techno-link.com
Phone: +35929817823

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K2Y24Q7XGHKZ2VT371RMR62K

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

zh013/5/en/0103800228241998
Oxiultra03800228240465