← Back to catalogue

GammaPro Slim Straight

EUDAMED

Class IIa (EU MDR)

Ref K0018C01

by Kub Technologies Inc

Identity

Trade Name
GammaPro Slim Straight EUDAMED
Device Name
GammaPro Slim Straight EUDAMED
Model / Reference
K0018C01 EUDAMED

Identifiers

Primary DI / UDI-DI
+B619K0018C010O EUDAMED
Basic UDI-DI
++B619K0018C01UP EUDAMED
Direct Marketing DI
+B619K0018C010O 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 Straight 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

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

Manufacturer

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

Sources (1)

  • EUDAMED a4fc6069-f382-48ee-84dc-48c5342b31db 61 fields · synced Jun 17, 2026