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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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Fili di Kirschner — 58 UDI-DI variants, MDR (BRM Extremities S.r.l.)

MD Atlas
BRM Extremities S.r.l.

Data from EUDAMED, last updated May 31, 2026

Fili di Kirschner

805771755FT09B5CB

58 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BRM Extremities S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805771755FT09B5CB
Device name: Fili di Kirschner
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: BRM Extremities S.r.l.
SRN: IT-MF-000016087
Country: Italy
Email: info@brm-extremities.com
Phone: +3903411693087

Variants by status

UDI-DI variants

58 UDI-DI variants

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Applied filters

basicUdiUlid01K9SP4RJWXZF7YD6969YPJM4N

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

STOIKW16201503N08053782780747
STOIKW16201510N08053782780990
STOIKW16200003N08053782780723
STOIKW16200010N08053782780976
STOIKW20200003N08053782780754
STOIKW20200010N08053782781003
STOIKW25200003N08053782780761
STOIKW25200010N08053782781010

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