FDA UDI In Commercial Distribution 🇺🇸 United States

Pro-Mag™ Biopsy Needle

DI: 00886333006915 · Model: 765018250 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Mag™ Biopsy Needle
Primary DI
00886333006915
Version / Model
765018250
Catalog Number
765018250
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
799d213a-5c6c-46f6-ab8d-d1a5292c48ea

Device Description

Pro-Mag™ Biopsy Needle 18ga x 25cm

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
47540 Soft-tissue biopsy needle, single-use

Identifiers

Type ID
Package 20886333006919
Primary 00886333006915

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 18ga x 25cm