Primary Device ID | B09921001400 |
NIH Device Record Key | 304a8f24-5fd5-4625-a22d-d793bdd7c133 |
Commercial Distribution Discontinuation | 2018-06-22 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | COOLEY AORTIC CLAMP |
Version Model Number | 2100-140 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, 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 | false |
Lot Batch | false |
Serial Number | false |
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 | 8008217496 |
INFO@SONTECINSTRUMENTS.COM | |
Phone | 8008217496 |
INFO@SONTECINSTRUMENTS.COM |
Length | 10.25 Inch |
Length | 10.25 Inch |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B09921001400 [Primary] |
DXC | Clamp, Vascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09921001400]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[B09921001400]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-08-08 |
B09921001500 | COOLEY AORTIC CLAMP CURVED JAW CURVED SHANK |
B09921001520 | COOLEY AORTIC CLAMP DOUBLE CURVED JAW CURVED SHANK |
B09921001400 | COOLEY AORTIC CLAMP DOUBLE ANGLED JAW CURVED SHANK |