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Retrax FS Solution

EUDAMED

Class I (EU MDR)

Ref 18520

by Pascal Company Inc.

Identity

Device Name
Retrax FS Solution EUDAMED
Model / Reference
18520 EUDAMED

Identifiers

Primary DI / UDI-DI
00310866002743 EUDAMED
Basic UDI-DI
003108665005XU EUDAMED
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Category: Gingival retraction cord, non-medicated

Retrax FS Solution by Pascal Company, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Pascal Company Inc.
EUDAMED SRN
US-MF-000032036
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED e26644b2-5812-47f6-8ef6-06fe8851e68b 61 fields · synced Jun 18, 2026