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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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BIOSYNEX AMPLIQUICK STI Panel I — 3 UDI-DI variants, IVDR (BIOSYNEX)

MD Atlas
BIOSYNEX

Data from EUDAMED, last updated May 19, 2026

BIOSYNEX AMPLIQUICK STI Panel I

353267F00204P7T

3 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: BIOSYNEX

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 353267F00204P7T
Device name: —
Device model: BIOSYNEX AMPLIQUICK STI Panel I
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOSYNEX
SRN: FR-MF-000014073
Country: France
Email: reglementaire@biosynex.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJZ5QA6JS59D3HQR0877RZEW

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

3150070_BLK10003532670103592
3150070_SEC0203532670103585
3150070_SEC0103532670103578