Primary Device ID | 00685447015376 |
NIH Device Record Key | 7a447934-63d1-4bc1-bca0-44319a76224f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Electrophysiology Cable |
Version Model Number | DEX-14 |
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 |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Length | 2.3 Meter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00685447015376 [Primary] |
DRF | Catheter, Electrode Recording, Or Probe, Electrode Recording |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-22 |
Device Publish Date | 2022-11-14 |
00685447015369 | 10 pin |
00685447015376 | 14 pin |