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Reamers

EUDAMED

Class IIa (EU MDR)

Ref A330 650 922 2502 030Model File Type K(SS304)/K Files、File Type H(SS304)/H Files、Reamer Type K(SS304)/Reamers etc

by Shanwei Perfect Medical Instruments Co., Ltd.

Identity

Trade Name
Reamers EUDAMED
Device Name
Dental Root-Canal Instruments EUDAMED
Model / Reference
File Type K(SS304)/K Files、File Type H(SS304)/H Files、Reamer Type K(SS304)/Reamers etc EUDAMED
A330 650 922 2502 030 EUDAMED

Identifiers

Primary DI / UDI-DI
06942200949700 EUDAMED
Basic UDI-DI
697590932SSTHandfilesJ4 EUDAMED
EMDN Code
Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Reamers by Shanwei Perfect Medical Instruments Co., Ltd. — Class IIa — 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
CN-MF-000033003
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 7f493ed5-4aa8-4101-81cb-684bb18cdb2a 61 fields · synced Jun 11, 2026