← Back to catalogue

Testi10™

EUDAMED

Class IIb (EU MDR)

Ref TESTIF-XLModel Size: XLarge (32*51 mm)

by Rigicon, Inc.

Identity

Trade Name
Testi10™ EUDAMED
Device Name
Testi10™ Firm Testicular Prosthesis EUDAMED
Model / Reference
Size: XLarge (32*51 mm) EUDAMED
TESTIF-XL EUDAMED

Identifiers

Primary DI / UDI-DI
00850299008146 EUDAMED
Basic UDI-DI
B-00850299008146 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 4af1cd4b-08b9-49f0-a5f5-4209e3555570 61 fields · synced Jun 18, 2026