Data from EUDAMED, last updated May 30, 2026

Sapphire II PRO

B-08717853296840

1 reference

Class III

Data from EUDAMED, last updated May 30, 2026

B-08717853296840

1 reference

Class III

Device family identification

Device name: Sapphire II PRO
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-08717853296840
Device model: Ø 3.0 x 10 mm
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: EUDAMED
Version date: Feb 25, 2022

Name: OrbusNeich Medical, B.V.
SRN An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor. View in glossary →: NL-MF-000010907
Country: Netherlands
Email: onra@orbusneich.com
Phone: +31 33 254 1150

No device characteristics flagged

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

Device family identification

Device name: Sapphire II PRO
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: B-08717853296840
Device model: Ø 3.0 x 10 mm
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: EUDAMED
Version date: Feb 25, 2022

References

1 reference

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Sapphire II PRO	`230-103-5U`	`08717853296840`	1	On the market