FDA UDI Not in Commercial Distribution 🇺🇸 United States

Multi Purpose Biopsy Kit

DI: 00886333208357 · Model: 195110 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Multi Purpose Biopsy Kit
Primary DI
00886333208357
Version / Model
195110
Catalog Number
195110
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-19
Public Version
2
Public Version Date
2024-01-30
Public Version Status
Update
Public Device Record Key
5f7cc345-c783-488c-bcdf-4e20a0fd94f6
Distribution End Date
2024-01-29

Device Description

Multi Purpose Biopsy Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
OJT Aspiration Tray

GMDN Terms

Code Name
61922 Soft-tissue biopsy procedure kit, medicated

Identifiers

Type ID
Package 20886333208351
Primary 00886333208357

Customer Contacts