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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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MEMOCERVICAL — 10 UDI-DI variants, MDR (BIOSYNEX)

MD Atlas
BIOSYNEX

Data from EUDAMED, last updated May 19, 2026

MEMOCERVICAL

353267F00193O8U

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: BIOSYNEX

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 353267F00193O8U
Device name: —
Device model: MEMOCERVICAL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 12, 2023

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01HGBA72FP84C1H4BTNPMZ69Q4

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

MEMOCERVICAL08055517560501
MEMOCERVICAL03532678604831
86048103532678604817
302108055517560495
86046303532678604633
MEMOCERVICAL03532678604848
MEMOCERVICAL08055517560723
MEMOCERVICAL08055517560129
MEMOCERVICAL03532678604640
86048203532678604824