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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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BlauProtect — 8 UDI-DI variants, MDR

MD Atlas
Synkotech Biocompatible Materials S.L

Data from EUDAMED, last updated May 23, 2026

BlauProtect

8437025406BPG6

8 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: Synkotech Biocompatible Materials S.L

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437025406BPG6
Device name: BlauProtect
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 3, 2025

Manufacturer & authorised representative

Manufacturer

Name: Synkotech Biocompatible Materials S.L
SRN: ES-MF-000031010
Country: Spain
Email: info@synkotechbio.com
Phone: +34 877 07 71 50

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01K6N5B89PM81PE4EE8H52JZNR

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

BP_ADVPLUS08437025406777
BP_SPRAY10008437025406104
BP_SPONGE308437025406005
BP_SPONGE108437025406142
BLAU_PROTECT08437025406845
BP_SPRAY20008437025406111
BP_SPRAY2584370254060986
BP_WIPE108437025406302