DEVICE: Brevera Breast Biopsy System (15420045507760)
Device Identifier (DI) Information
Brevera Breast Biopsy System
BREVDRV
In Commercial Distribution
BREVDRV
Hologic, Inc.
BREVDRV
In Commercial Distribution
BREVDRV
Hologic, Inc.
The reusable device driver is the electromechanical component of the Brevera(R) (R) Breast Biopsy system.
Device Characteristics
MR Unsafe | |
No | |
No | |
No | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
36190 | Mammographic stereotactic biopsy system |
An assembly of devices intended to be used in conjunction with mammography to insert biopsy devices, typically designated needles, into a breast in order to extract a biopsy of a suspect tumour for diagnostic purposes. It consists of a biopsy unit with needle guides, needles, an examination table, and an integral computer for communicating lesion coordinates. This GMDN code includes stand-alone units as well as units that mount onto an existing mammographic radiographic unit.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
KNW | INSTRUMENT, BIOPSY |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K163052 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Storage Environment Temperature: between -10 and 60 Degrees Celsius |
Storage Environment Atmospheric Pressure: between 697 and 1013 millibar |
Storage Environment Humidity: between 10 and 80 Percent (%) Relative Humidity |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
43841c2e-004c-4a16-b6e9-72cf5c10c337
April 19, 2024
3
August 28, 2018
April 19, 2024
3
August 28, 2018
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
25420045507767 | 1 | 15420045507760 | In Commercial Distribution | BOX |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)442-9892
CustomerSupport@hologic.com
CustomerSupport@hologic.com