FDA UDI In Commercial Distribution 🇺🇸 United States

Vesseloop™

DI: 00886333222490 · Model: 001-1-110 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Vesseloop™
Primary DI
00886333222490
Version / Model
001-1-110
Catalog Number
001-1-110
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2020-05-06
Public Version Status
Update
Public Device Record Key
f858c3c9-c30d-4605-9cda-9710184f6a98

Device Description

Vesseloop™ Silicone Vascular Ties Radiopaque, Red Mini

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
DXC Clamp, Vascular

GMDN Terms

Code Name
61916 Surgical vessel loop

Identifiers

Type ID
Package 20886333222494
Primary 00886333222490

Customer Contacts