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Retraction Cord

EUDAMED

Class I (EU MDR)

Ref 010/0038Ref 010/0042Ref 010/0041Ref 010/0040

by Perfection Plus

Identity

Device Name
Retraction Cord EUDAMED
Model / Reference
010/0038 EUDAMED
010/0042 EUDAMED
010/0041 EUDAMED
010/0040 EUDAMED

Identifiers

Primary DI / UDI-DI
05060660619344 EUDAMED
05060660616633 EUDAMED
05060660616626 EUDAMED
05060660616619 EUDAMED
Basic UDI-DI
506066061TFPP008CJ EUDAMED
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Retraction Cord by Perfection Plus — 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
Perfection Plus
EUDAMED SRN
GB-MF-000023781
Authorised Representative
Advena Limited MT-AR-000000234

Sources (4)

  • EUDAMED 5ce9d220-bb77-45c6-990e-946d5aaf1a87 61 fields · synced Sep 18, 2026
  • EUDAMED 8c3db76c-4fdc-4aaa-b8f7-81074dd9eb64 61 fields · synced May 18, 2026
  • EUDAMED f6dfe855-293c-4e7c-b752-67f4fb736e19 61 fields · synced May 18, 2026
  • EUDAMED 935c1019-2857-4700-9d73-5447d1a44516 61 fields · synced May 18, 2026