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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 — 1 UDI-DI variant, MDD (G21 S.R.L.)

MD Atlas
G21 S.R.L.

Data from EUDAMED, last updated May 30, 2026

SpaceFlex Hip

B-08058964726889

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: G21 S.R.L.

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Device characteristics

Implantable

Legacy certificates

Certificate number: MED 28029_1
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: KIWA CERMET ITALIA S.P.A. (0476)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08058964726889
Device name: SpaceFlex Hip
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Mar 24, 2026

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

1 UDI-DI variant

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basicUdiUlid01KMG88J409Q4BZHW4NA22T4YY

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 Hip08058964726889