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Mammotome Revolve™ Dual Vacuum-Assisted Breast Biopsy System

EUDAMED

Class I (EU MDR)

Ref MSMB1208

by Devicor Medical Products, Inc.

Identity

Trade Name
Mammotome Revolve™ Dual Vacuum-Assisted Breast Biopsy System EUDAMED
Device Name
Specimen Management System EUDAMED
Model / Reference
MSMB1208 EUDAMED

Identifiers

Primary DI / UDI-DI
00841911100836 EUDAMED
Basic UDI-DI
08419111AD02D000003322SD EUDAMED
EMDN Code
A019012 BREAST NODULES AND OTHER STRUCTURES LOCALISATION NEEDLES AND SYSTEMS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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

Mammotome Revolve™ Dual Vacuum-Assisted Breast Biopsy System by Devicor Medical Products, Inc. — Class I — MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000003322
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (1)

  • EUDAMED 142d1bee-418a-4262-92cb-c3d9b5bf3373 61 fields · synced Jul 19, 2026