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Root Elevator Flohr 3mm

EUDAMED

Class I (EU MDR)

Ref 3020304

by Lipuma

Identity

Device Name
Root Elevator Flohr 3mm EUDAMED
Model / Reference
3020304 EUDAMED

Identifiers

Primary DI / UDI-DI
G15830203040 EUDAMED
Basic UDI-DI
++G1583020304QD EUDAMED
Direct Marketing DI
G15830203040 EUDAMED
EMDN Code
L150301 DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Root Elevator Flohr 3mm by Lipuma — 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
Lipuma
EUDAMED SRN
PK-MF-000024322
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED ac61f7f6-ce4a-41ed-9e82-25266fb5282d 61 fields · synced Jun 19, 2026