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Lama Periotomo Angolare

EUDAMED

Class I (EU MDR)

Ref 868/2Model STRUMENTI CHIRURGICI RIUTILIZZABILI

by MEDESY srl

Identity

Trade Name
LAMA PERIOTOMO ANGOLARE EUDAMED
Model / Reference
STRUMENTI CHIRURGICI RIUTILIZZABILI EUDAMED
868/2 EUDAMED

Identifiers

Primary DI / UDI-DI
08056215744637 EUDAMED
Basic UDI-DI
805660060MEDFT01IMXF EUDAMED
Direct Marketing DI
08056215744637 EUDAMED
EMDN Code
L0914 SCOLLAPERIOSTIUM AND PERIOSTEOTOMES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Lama Periotomo Angolare by MEDESY srl — 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
MEDESY srl
EUDAMED SRN
IT-MF-000028737

Sources (1)

  • EUDAMED c5fef828-5069-4c2b-b9f8-76c595a24915 61 fields · synced Jun 18, 2026