FDA UDI In Commercial Distribution 🇺🇸 United States

VACORA®

DI: 00801741079672 · Model: VF2019 · Bard Peripheral Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VACORA®
Primary DI
00801741079672
Version / Model
VF2019
Catalog Number
VF2019
Company Name
Bard Peripheral Vascular, Inc.
Labeler DUNS
135057938
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2018-09-24
Public Version Status
Update
Public Device Record Key
5e7bb26a-24a9-4ad3-89ec-6aa670cde4d8

Device Description

VACORA® Vacuum Assisted Biopsy System

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KNW INSTRUMENT, BIOPSY

GMDN Terms

Code Name
36190 Mammographic stereotactic biopsy system

Identifiers

Type ID
Primary 00801741079672

Customer Contacts