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GammaPro Slim Angled

EUDAMED

Class IIa (EU MDR)

Ref K0021C01

by Kub Technologies Inc

Identity

Trade Name
GammaPro Slim Angled EUDAMED
Device Name
GammaPro Slim Angled EUDAMED
Model / Reference
K0021C01 EUDAMED

Identifiers

Primary DI / UDI-DI
+B619K0021C010I EUDAMED
Basic UDI-DI
++B619K0021C01TH EUDAMED
Direct Marketing DI
+B619K0021C010I EUDAMED
EMDN Code
Z11029001 BETA/GAMMA DETECTORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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: Hand-held-detector nuclear medicine system

GammaPro Slim Angled by Kub Technologies Inc — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held-detector nuclear medicine system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000026338
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED eb0cd209-8265-472d-81d5-d1591438f489 61 fields · synced Jun 18, 2026