FDA UDI In Commercial Distribution 🇺🇸 United States

Introducer Sheath/Needle

DI: 00886333001668 · Model: 19 ga x 20 cm · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Introducer Sheath/Needle
Primary DI
00886333001668
Version / Model
19 ga x 20 cm
Catalog Number
ISN 1920
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
8
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
93111d78-cb92-4214-9738-cd0aa997e4a2

Device Description

Introducer Sheath/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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FGE Catheter, Biliary, Diagnostic

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Primary 00886333001668
Package 20886333001662

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 19 ga x 20 cm