Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Non-Sterile Reusable Foreign Body… — 13 UDI-DI variants, MDR

MD Atlas
G-FLEX FLEXIBLE INSTRUMENTS EUROPE

Data from EUDAMED, last updated May 23, 2026

Non-Sterile Reusable Foreign Body Retrievers

54200513-TF20-FBR-RU-8U

13 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: G-FLEX FLEXIBLE INSTRUMENTS EUROPE

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 54200513-TF20-FBR-RU-8U
Device name: Non-Sterile Reusable Foreign Body Retrievers
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: G-FLEX FLEXIBLE INSTRUMENTS EUROPE
SRN: BE-MF-000000623
Country: Belgium
Email: thierry@g-flex.com
Phone: +3267883665

Variants by status

UDI-DI variants

13 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KMMK8N5XA4SWN655ZVY19TGR

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

Non-Sterile Reusable Foreign Body Retrievers05420051300235
Non-Sterile Reusable Foreign Body Retrievers05420051300228
Non-Sterile Reusable Foreign Body Retrievers05420051300082
Non-Sterile Reusable Foreign Body Retrievers05420051300167
Non-Sterile Reusable Foreign Body Retrievers05420051306527
Non-Sterile Reusable Foreign Body Retrievers05420051300198
Non-Sterile Reusable Foreign Body Retrievers05420051300068
Non-Sterile Reusable Foreign Body Retrievers05420051300266
Non-Sterile Reusable Foreign Body Retrievers05420051300099
Non-Sterile Reusable Foreign Body Retrievers05420051300051
Non-Sterile Reusable Foreign Body Retrievers05420051300259
Non-Sterile Reusable Foreign Body Retrievers05420051300181
Non-Sterile Reusable Foreign Body Retrievers05420051300150