Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Sredstva za uklapanje — 24 UDI-DI variants, IVDR (BioGnost Ltd.)

MD Atlas
BioGnost Ltd.

Data from EUDAMED, last updated May 24, 2026

Sredstva za uklapanje

385889212HPC30704EMBEP7

24 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: BioGnost Ltd.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 385889212HPC30704EMBEP7
Device name: Sredstva za uklapanje
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: BioGnost Ltd.
SRN: HR-MF-000022153
Country: Croatia
Email: ivan.marchiotti@biognost.hr
Phone: +38512409997

Variants by status

UDI-DI variants

24 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01G39T3K9F95NVF112KQEZ94Q0

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

BW52/54-103858888822552
BW52/54-1003858890000870
BW52/54-203858888822569
BW56/58-103858888822576
BW56/58-1003858888827694
BW56/58-203858888822583
BWB-103858888822590
BWB-1003858890000245
BWB-203858888822606
BWPLUS-103858888822637
BWPLUS-1003858888820312
BWPLUS-203858888822644
08-SPRAY-203858888829353
CryoFix Gel blue, 100 mL03858888823221
CryoFix Gel green, 100 mL03858888823238
CryoFix Gel pink, 100 mL03858888823214
CryoFix Gel yellow, 100 mL03858890003727
CF-10003858888823207
DeMold solution, 1000 mL03858888822064
DeMold solution, 500 mL03858888822057
DS-10003858888822040
MC-OT-10003858890009019
TS-1L03858890006018
TS-50003858890006001