Skip to content

Testi10™

by Rigicon, Inc. United States EUDAMED

Ref TESTIF-XSModel Size: XSmall (21*27 mm) EMDN P080201

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00850299008108 Basic UDI-DIDate19 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Testi10™ Firm Testicular Prosthesis
Model / Reference
Size: XSmall (21*27 mm), TESTIF-XS
Primary DI / UDI-DI
00850299008108
Basic UDI-DI
B-00850299008108
EMDN Code
P080201 Testicle prostheses
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
US-MF-000027758
Authorised representative
Rigicon B.V. NL-AR-000013173

Other devices from Rigicon, Inc.

See all devices from Rigicon, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 00850299008108|B-00850299008108 61 fields · synced 25 Oct 2026