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Scope-Pro Internal tube kit

EUDAMED

Class I (EU MDR)

Ref Q89ITKModel SPF

by Amity Limited

Identity

Trade Name
Scope-Pro Internal tube kit EUDAMED
Model / Reference
SPF EUDAMED
Q89ITK EUDAMED

Identifiers

Primary DI / UDI-DI
05060722252540 EUDAMED
Basic UDI-DI
506072225AAA0005JS EUDAMED
EMDN Code
Z12011380 CLEANING, DISINFECTION AND STERILISATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern 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

Scope-Pro Internal tube kit by Amity Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Amity Limited
EUDAMED SRN
GB-MF-000023321
Authorised Representative
Amity Healthcare EU Ltd. IE-AR-000011613

Sources (1)

  • EUDAMED f01e1554-961b-4c56-a5da-5173a1c56ec6 61 fields · synced Aug 1, 2026