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Mammotome Revolve

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref MSCM1

by Devicor Medical Products, Inc.

Identity

Trade Name
Mammotome Revolve™ Dual Vacuum-Assisted Breast Biopsy System EUDAMED
Mammotome Revolve FDA UDI
Generic Name
Mammographic stereotactic biopsy system FDA UDI
Device Name
Control Module EUDAMED
Mammotome Revolve Control Module- Python FDA UDI
Model / Reference
MSCM1 EUDAMEDFDA UDI
Description
Mammotome Revolve Control Module- Python FDA UDI

Identifiers

Catalog Number
CA000606003 FDA UDI
Primary DI / UDI-DI
00841911103165 EUDAMEDFDA UDI
Basic UDI-DI
08419111AD02A000003322PN EUDAMED
FDA Product Code
KNW FDA UDI
EMDN Code
A019012 BREAST NODULES AND OTHER STRUCTURES LOCALISATION NEEDLES AND SYSTEMS EUDAMED
GMDN Term
Mammographic stereotactic biopsy system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mammographic stereotactic biopsy system

Mammotome Revolve by Devicor Medical Products, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Mammographic stereotactic biopsy system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 460c5705-83b3-490c-a9a5-ba994a18d063 34 fields · synced Jul 10, 2026
  • EUDAMED dc9917ad-395a-4b28-af20-826c919deac5 61 fields · synced Jul 10, 2026