FDA UDI Not in Commercial Distribution 🇺🇸 United States

VersaCross Steerable Access Solution

DI: 00685447017936 · Model: VSTK0009 · Baylis Médicale Cie Inc
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VersaCross Steerable Access Solution
Primary DI
00685447017936
Version / Model
VSTK0009
Company Name
Baylis Médicale Cie Inc
Labeler DUNS
249225954
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-27
Public Version
3
Public Version Date
2023-12-08
Public Version Status
Update
Public Device Record Key
29862c62-8b43-4c5a-8c9e-7ad4c9a3b012
Distribution End Date
2023-02-05

Device Description

1 x VersaCross Steerable Sheath (including 1 x Dilator and 1 x J-tip Guidewire); 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use))

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
DXF Catheter, Septostomy
DYB Introducer, Catheter

GMDN Terms

Code Name
47247 Cardiac transseptal access set

Identifiers

Type ID
Primary 00685447017936

Customer Contacts

Phone
5144889801

Device Sizes

Type Value Unit Text
Device Size Text, specify 72cm 8.5F VersaCross Steerable Sheath with Medium Curl (incl. 95cm Standard Curve D0 Dilator; 180cm J-Tip Guidewire OD=0.035in); 230cm J-Tip VersaCross RF Wire OD=0.035in (10ft(3m) Connector Cable)