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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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Cystoflex™ Standard Deflection — 2 UDI-DI variants, MDR

MD Atlas
Axess Vision Technology

Data from EUDAMED, last updated May 19, 2026

Cystoflex™ Standard Deflection

3664977EMDNZ12020701P8

2 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: Axess Vision Technology

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3664977EMDNZ12020701P8
Device name: Cystoflex™ Standard Deflection
Device model: 11010011
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Axess Vision Technology
SRN: FR-MF-000003039
Country: France
Email: raqa.ptm@tsc-group.com
Phone: +31 33 450 7250

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMMPKR67P7FA0EE9ZFBNS94S

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

1101001203664977000066
1101001103664977000059