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Apex

EUDAMED

Class I (EU MDR)

Ref 2S01229

by Falcon Surgical Co. (Pvt.) Ltd

Identity

Trade Name
Apex EUDAMED
Device Name
PROBES EUDAMED
Model / Reference
2S01229 EUDAMED

Identifiers

Primary DI / UDI-DI
+G1202S012290I EUDAMED
Basic UDI-DI
++G120PPROBE3N EUDAMED
EMDN Code
L159003 DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Apex by Falcon Surgical Co. (Pvt.) Ltd — 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

EUDAMED SRN
PK-MF-000018125
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ce3dcd4a-c1d8-478c-b69e-7e78f6517140 61 fields · synced Sep 18, 2026