Primary Device ID | 20685447001021 |
NIH Device Record Key | d4f171c6-dfc2-4f77-83a2-d2490960ffd9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Adult Dispersive Electrode |
Version Model Number | RFA-GP-BAY |
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 | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com | |
Phone | 5144889801 |
info@baylismedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00685447001027 [Primary] |
GS1 | 10685447001024 [Package] Contains: 00685447001027 Package: [25 Units] In Commercial Distribution |
GS1 | 20685447001021 [Package] Contains: 10685447001024 Package: [4 Units] In Commercial Distribution |
JOS | Electrode, Electrosurgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-02-03 |
00685447020080 - VersaCross Connect™ | 2024-08-28 Access Solution for CARTO VIZIGO™ Sheath |
00685447020103 - VersaCross Connect™ | 2024-08-28 Access Solution for CARTO VIZIGO™ Sheath |
00685447019046 - VersaCross Connect Access Solution for FARADRIVE | 2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use)) |
00685447019053 - VersaCross Connect Access Solution for FARADRIVE | 2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use)) |
00685447019060 - VersaCross Connect Access Solution for FARADRIVE | 2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use)) |
00685447019077 - VersaCross Connect Access Solution for FARADRIVE | 2024-01-19 1 x VersaCross Connect Transseptal Dilator; 1 x VersaCross RF Wire (including 1 x Connector Cable (Single Use)) |
00685447005964 - SupraCross Steerable Sheath | 2023-11-16 SupraCross Steerable Sheath; Transseptal Dilator; J-Tip Guidewire |
00685447005971 - SupraCross Steerable Sheath | 2023-11-16 SupraCross Steerable Sheath; Transseptal Dilator; J-Tip Guidewire |