← Back to catalogue

Silavit

EUDAMED

Class I (EU MDR)

Ref SilavitModel 188962 / 18-3362

by Aso Llc

Identity

Trade Name
Silavit EUDAMED
Device Name
Nasal Dilator Triple Bridge Tan P2S EUDAMED
Model / Reference
188962 / 18-3362 EUDAMED
Silavit EUDAMED

Identifiers

Primary DI / UDI-DI
02200286337236 EUDAMED
Basic UDI-DI
0017276188962S4 EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Silavit by Aso LLC — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

Manufacturer
Aso Llc
EUDAMED SRN
US-MF-000008641
Authorised Representative
Aso Europe BV NL-AR-000004377

Sources (1)

  • EUDAMED e24fa218-bb34-4199-afdd-ca0de72ab655 61 fields · synced Jun 18, 2026