FDA UDI In Commercial Distribution 🇺🇸 United States

EVIVA_0910-12

DI: 15420045504936 · Model: EVIVA_0910-12 · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
EVIVA_0910-12
Primary DI
15420045504936
Version / Model
EVIVA_0910-12
Catalog Number
EVIVA_0910-12
Company Name
Hologic, Inc.
Labeler DUNS
018925968
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-26
Public Version
6
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
3ca1ba57-b5d1-46f3-9d17-de3a5fc50a82

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
Yes
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
No
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 15420045504936
Package 35420045504930
Package 25420045504933

Premarket Submissions

Submission Number Supplement Number
K180233 000