FDA UDI In Commercial Distribution 🇺🇸 United States

Percutaneous Micro-Introducer Kit

DI: 00886333215010 · Model: 497811 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Percutaneous Micro-Introducer Kit
Primary DI
00886333215010
Version / Model
497811
Catalog Number
497811
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7e89dffd-40af-4fa3-91cd-8179e5389d80

Device Description

4F Percutaneous Micro-Introducer 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
OFL Percutaneous Sheath Introducer Kit

GMDN Terms

Code Name
46488 Magnetocardiography system

Identifiers

Type ID
Package 10886333215017
Primary 00886333215010
Package 20886333215014

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4F