FDA UDI In Commercial Distribution 🇺🇸 United States

Sertera Biopsy Device

DI: 25420045504063 · Model: Sertera-14 · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sertera Biopsy Device
Primary DI
25420045504063
Version / Model
Sertera-14
Catalog Number
Sertera-14
Company Name
Hologic, Inc.
Labeler DUNS
018925968
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-14
Public Version
4
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
e8975db1-3560-41e5-a7e3-f72cc8bb0787

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
KNW INSTRUMENT, BIOPSY

GMDN Terms

Code Name
58990 Side-notch biopsy gun handpiece/needle

Identifiers

Type ID
Primary 25420045504063

Premarket Submissions

Submission Number Supplement Number
K150169 000