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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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G21 S.R.L. — Manufacturer in Italy

EUDAMED update: Aug 5, 2025

G21 S.R.L.

IT-MF-000030085

Active

Address: via Sandro Pertini, 8 41039 San Possidonio
Role: Manufacturer
Date of registration: Oct 27, 2022
Country: IT Italy

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Device families (Basic UDI-DI) of G21 S.R.L.

Showing 1–15 of 15 device families.

SpaceFlex Hip Instrument Kit0805896472spaceflexHE
Winch Kyphoplasty Balloon Catheter 11G 20mmB-08058964726773
Disp. Mixing Bowl-OB-08058964723758
SpaceFlex HipB-08058964726889
SpaceFlex HipB-08058964727220
SpaceFlex HipB-08058964727237
SpaceFlex HipB-08058964726902
KeyFix Bone Cement Filler Cannula for Screw CementationB-08058964724441
KeyFix Bone DrillB-08058964724427
G1 40B-08058964723970
G1 40B-08058964727053
G3 20B-08058964720030
G3 20B-08058964727060
G3 40B-08058964720047
G3 40B-08058964727077

Certificate health for G21 S.R.L.

No certificates registered for this manufacturer.

Statistics for G21 S.R.L.

71Total Devices

68Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

8Countries

Market presence of G21 S.R.L.

Devices placed in 8 countries

Italy56
Türkiye5
Spain3
Bulgaria2
Germany2
France1
Netherlands1
Portugal1

Devices by risk class

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About G21 S.R.L.

SRN: IT-MF-000030085
Role: Manufacturer
Country: Italy
Organization name: G21 S.R.L.
EU VAT number: 03208750368
EORI: IT03208750368
Trade register: MO-368109
Date of registration: Oct 27, 2022

Contact details for G21 S.R.L.

Address: 8, VIA SANDRO PERTINI 41039 SAN POSSIDONIO ITALY
Phone: +39 0535 30312
Email: info@g-21.it
Website: www.g-21.it

Validator

Name: Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
SRN: IT-CA-070
Phone: +39 06 5994 3199/ +39 06 5994 3207
Email: segr.dgfdm@sanita.it

Officers and regulatory representatives of G21 S.R.L.

FORONI Maurizio
-conformity of the devices, in accordance with quality management system; -technical documentation and EU DoC are drawn up an kept up-to-date; -post-market surveillance obligations are complied; -vigilance reporting obligations are fulfilled; -in case of investigational devices, statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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Device catalog for G21 S.R.L.

No devices registered for this manufacturer.