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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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SpaceFlex Hip Instrument Kit — 4 UDI-DI variants, MDR (G21 S.R.L.)

MD Atlas
G21 S.R.L.

Data from EUDAMED, last updated May 30, 2026

SpaceFlex Hip Instrument Kit

0805896472spaceflexHE

4 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: G21 S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0805896472spaceflexHE
Device name: SpaceFlex Hip Instrument Kit
Device model: 900008
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: G21 S.R.L.
SRN: IT-MF-000030085
Country: Italy
Email: info@g-21.it
Phone: +39 0535 30312

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJQ2BTJ91FN8A5BK00WXW9AX

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

SpaceFlex Hip Instrument Kit08058964727268
90000808058964726186
90001208058964726797
SpaceFlex Shoulder Instrument Kit08058964727251