FDA UDI In Commercial Distribution 🇺🇸 United States

ViperCath XC

DI: 10852528005688 · Model: 035-XC-200-0 · Cardiovascular Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ViperCath XC
Primary DI
10852528005688
Version / Model
035-XC-200-0
Catalog Number
7-10043-01
Company Name
Cardiovascular Systems, Inc.
Labeler DUNS
024954518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-04
Public Version
4
Public Version Date
2023-12-25
Public Version Status
Update
Public Device Record Key
8b77d92b-9964-4a14-9186-5446a94d34e5

Device Description

200 cm, 0.035" guidewire compatible, support catheter

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
DQY Catheter, Percutaneous

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 10852528005688

Customer Contacts

Phone
877-274-0360
Phone
651-259-1600

Device Sizes

Type Value Unit Text
Device Size Text, specify Max Outer Diameter: 0.059 inches
Device Size Text, specify Inner Diameter: 0.035 inches
Device Size Text, specify Length: 200 cm