FDA UDI In Commercial Distribution 🇺🇸 United States

Vein360 Reprocessed Digital Intravascular (IVUS) Reprocessed Catheter PV .018

DI: 00850065047010 · Model: 86700RH · Vein360 LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vein360 Reprocessed Digital Intravascular (IVUS) Reprocessed Catheter PV .018
Primary DI
00850065047010
Version / Model
86700RH
Catalog Number
86700RH
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
ba947f54-cb68-4d23-bef7-9161c3810aa9

Device Description

Vein360 Reprocessed Digital Intravascular (IVUS) Reprocessed Catheter PV .018 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 00850065047010

Premarket Submissions

Submission Number Supplement Number
K230928 000