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Dodaci hranjivim podlogama - EUDAMED Registration 03858892125007

Access comprehensive regulatory information for Dodaci hranjivim podlogama in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 03858892125007 and manufactured by BioGnost Ltd. in Croatia.

This page provides complete registration details including trade name (BioSap HO, 50 mL), manufacturer information, competent authority (Agencija za lijekove i medicinske proizvode), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class A
03858892125007
No
Dodaci hranjivim podlogama
Trade Name: BioSap HO, 50 mL
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Device Description (EMDN)

ADDITIVES FOR DCM (GROWTH SUPPLEMENTS, SELECTIVE AGENTS, ...)

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W0104010104
Trade Name
BioSap HO, 50 mL
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
03858892125007
Basic UDI
385889212BAC4010104SUQL
Version Date
October 11, 2024
Manufacturer Last Update
September 20, 2022
Active Status
No
Manufacturer
Manufacturer Name
BioGnost Ltd.
Country
Croatia
Country Type
EU_MEMBER_STATE
Address
59 Medjugorska Zagreb
Email
mirjana.ulip@biognost.hr
Regulatory Information
Competent Authority
Agencija za lijekove i medicinske proizvode
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Croatia
Market Available
Bulgaria:None~None, Croatia:None~None, Greece:None~None, Italy:None~None, Slovenia:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
Yes