Primary Device ID | 00685447018841 |
NIH Device Record Key | f3c03070-5049-45ac-a5cf-8be17d1aa179 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VersaCross Connect Transseptal Dilator |
Version Model Number | VXA12-84-35-PS-D1 |
Catalog Number | NA |
Company DUNS | 249225954 |
Company Name | Baylis Médicale Cie Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00685447018841 [Primary] |
DRE | Dilator, Vessel, For Percutaneous Catheterization |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-23 |
Device Publish Date | 2023-08-15 |
00685447010531 | 1 x VersaCross Connect Transseptal Dilator; 1 x J-Tip Guidewire (Single Use) |
00685447010487 | 1 x VersaCross Connect Transseptal Dilator; 1 x J-Tip Guidewire (Single Use) |
00685447018841 | 1 x VersaCross Connect Transseptal Dilator (Single Use) |