FDA UDI In Commercial Distribution 🇺🇸 United States

SuperCore™ Biopsy Instrument

DI: 00886333006014 · Model: 701216090 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SuperCore™ Biopsy Instrument
Primary DI
00886333006014
Version / Model
701216090
Catalog Number
701216090
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
3
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
7b13a317-7404-4b8a-9625-ad52411b5632

Device Description

SuperCore™ Biopsy Instrument with Co-Axial Introducer Needle

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KNW Instrument, Biopsy

GMDN Terms

Code Name
22726 End-cut biopsy gun handpiece/needle

Identifiers

Type ID
Package 20886333006018
Primary 00886333006014

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Co-Axial Introducer Needle: 15ga x 3.9cm
Device Size Text, specify SuperCore: 16ga x 9cm