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Guide Reamer

EUDAMED

Class I (EU MDR)

Ref SGRE52

by SEWONMEDIX Inc.

Identity

Trade Name
Guide Reamer EUDAMED
Device Name
IH IMPLANT SYSTEM / Laboratory components & Etc. EUDAMED
Model / Reference
SGRE52 EUDAMED

Identifiers

Primary DI / UDI-DI
08800041364343 EUDAMED
Basic UDI-DI
8800041300003014W EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Guide Reamer by SEWONMEDIX Inc. — 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
SEWONMEDIX Inc.
EUDAMED SRN
KR-MF-000016194
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED c288bbbf-bff1-48c5-a321-adf52e42d5e4 61 fields · synced Jun 18, 2026