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Mammotome MR

FDA UDI

Class II (US FDA UDI)

by Devicor Medical Products, Inc.

Identity

Trade Name
Mammotome MR FDA UDI
Generic Name
Mammographic stereotactic biopsy system FDA UDI
Device Name
MR Targeting Set - Short FDA UDI
Model / Reference
MRT08S FDA UDI
Description
MR Targeting Set - Short FDA UDI

Identifiers

Catalog Number
MRT08S FDA UDI
Primary DI / UDI-DI
00841911101048 FDA UDI
510(k) Number
K042753 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Mammographic stereotactic biopsy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Height — 115 Millimeter FDA UDI
Needle Gauge — 8 Gauge FDA UDI

Category: Mammographic stereotactic biopsy system

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

Similar devices

Also classified as Mammographic stereotactic biopsy system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d9c319c-a0cf-4a17-b1bb-5efff1eb5e5c 37 fields · synced Jun 8, 2026