Primary Device ID | 03701089514231 |
NIH Device Record Key | c075cc5f-4c49-417f-a2db-67d6e60395ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VENTO Cup |
Version Model Number | 1-01-12-3960 |
Company DUNS | 634855407 |
Company Name | AMPLITUDE SAS |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com | |
Phone | +0033475418741 |
regulatoryaffairs@amplitude-ortho.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03701089514231 [Primary] |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2017-12-05 |