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Atec Emerald

FDA UDI

Class II (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
ATEC EMERALD FDA UDI
Generic Name
Mammographic stereotactic biopsy system FDA UDI
Device Name
BREAST BIOPSY SYSTEM FOR BIOPSIES UNDER MRI FDA UDI
Model / Reference
ATEC EMERALD FDA UDI
Description
BREAST BIOPSY SYSTEM FOR BIOPSIES UNDER MRI FDA UDI

Identifiers

Catalog Number
ATEC EMERALD FDA UDI
Primary DI / UDI-DI
15420045506848 FDA UDI
510(k) Number
K042290 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Mammographic stereotactic biopsy system

Atec Emerald by Hologic, 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

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI f8a10858-780f-4819-9577-893f3b3be4c2 36 fields · synced May 30, 2026