Primary Device ID | 00816396022164 |
NIH Device Record Key | fefe150c-c65f-463f-8502-84876c2b6b8b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UPMM |
Version Model Number | 3060-01-01 |
Catalog Number | 3060-01-01 |
Company DUNS | 109132019 |
Company Name | IVY BIOMEDICAL SYSTEMS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 203-481-4183 |
sales@ivybiomedical.com | |
Phone | 203-481-4183 |
sales@ivybiomedical.com | |
Phone | 203-481-4183 |
sales@ivybiomedical.com |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Height | 2.5 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816396022164 [Primary] |
DRT | Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-14 |
00816396022164 | Cardiac Gating Module |
00816396022157 | Cardiac Gating Module |
00816396020825 | Cardiac Gating Module & Accessory Kit |
00816396020818 | Cardiac Gating Module & Accessory Kit |