FDA UDI In Commercial Distribution 🇺🇸 United States

Speed-Torque®

DI: 00860003987353 · Model: VSXT001 · Vascugenix, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Speed-Torque®
Primary DI
00860003987353
Version / Model
VSXT001
Company Name
Vascugenix, LLC
Labeler DUNS
117166275
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-03
Public Version
1
Public Version Date
2022-11-11
Public Version Status
New
Public Device Record Key
288f5ca2-c23c-4db3-afb6-ad58bce0300a

Device Description

Speed-Torque® Device Pouch

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
Radiation Sterilization

Product Codes

Code Name
PTL Wire, Guide, Catheter, Exempt

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Package 10860003987350
Primary 00860003987353
Package 20860003987357

Customer Contacts

Phone
5015008025