FDA UDI In Commercial Distribution 🇺🇸 United States

Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter

DI: 00850065047058 · Model: 85900PSTRH · Vein360 LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter
Primary DI
00850065047058
Version / Model
85900PSTRH
Catalog Number
85900PSTRH
Company Name
Vein360 LLC
Labeler DUNS
080926907
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-02
Public Version
1
Public Version Date
2024-08-12
Public Version Status
New
Public Device Record Key
ac0a8ccc-7174-4bd2-979c-6c13ac0388cd

Device Description

Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter for Medline Renewal

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
Yes
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
OWQ Reprocessed Intravascular Ultrasound Catheter

GMDN Terms

Code Name
64174 Intravascular ultrasound imaging catheter, reprocessed

Identifiers

Type ID
Primary 00850065047058

Premarket Submissions

Submission Number Supplement Number
K232584 000