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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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LABORATORY SCREW — 10 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 23, 2026

LABORATORY SCREW

84353898LAB-SCREWGX

10 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: 84353898LAB-SCREWGX
Device name: LABORATORY SCREW
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 9, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K74R2TQV3R82TBD27KNJ4WRJ

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

INTEIU08435389804260
TEIU1508435389805366
TEMIR1208435389820444
TEMIR08435389810018
INTEPESPE08435389819974
TEMIR2008435389820451
INTEIU1608435389805359
TEIT08435389803454
INTTLH08435389804802
TTLH08435389803256