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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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STERILIZATION BOX — 7 UDI-DI variants, MDR

MD Atlas
B.T.I. BIOTECHNOLOGY INSTITUTE, S.L

Data from EUDAMED, last updated May 23, 2026

STERILIZATION BOX

84353898STERI-CONTAINERFY

7 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: B.T.I. BIOTECHNOLOGY INSTITUTE, S.L

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84353898STERI-CONTAINERFY
Device name: STERILIZATION BOX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: B.T.I. BIOTECHNOLOGY INSTITUTE, S.L
SRN: ES-MF-000001701
Country: Spain
Email: technicalmanager@bti-implant.es

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K5GTAHNKH9KYHAKCMBPDVYV2

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

CEXCO08435389825265
CCG3008435389827306
CQ508435389821960
CCG08435389830207
CEXIM08435389812692
CQ108435389809586
CP108435389805557