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Testi10™

EUDAMED

Class IIb (EU MDR)

Ref TESTISF-MModel Size: Medium (29*41 mm)

by Rigicon, Inc.

Identity

Trade Name
Testi10™ EUDAMED
Device Name
Testi10™ Saline-Filled Testicular Prosthesis EUDAMED
Model / Reference
Size: Medium (29*41 mm) EUDAMED
TESTISF-M EUDAMED

Identifiers

Primary DI / UDI-DI
00850299008078 EUDAMED
Basic UDI-DI
B-00850299008078 EUDAMED
EMDN Code
P080201 TESTICLE PROSTHESES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Testi10™ by Rigicon, Inc. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Rigicon, Inc.
EUDAMED SRN
US-MF-000027758
Authorised Representative
Rigicon B.V. NL-AR-000013173

Sources (1)

  • EUDAMED 6ae25f86-01d0-4105-b205-5b8bb6a2a236 61 fields · synced Jun 20, 2026