Primary Device ID | B09921002300 |
NIH Device Record Key | 38ebcb6c-4341-4698-abe4-9bd71c1b7d65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COOLEY MULTI PURPOSE CLAMP |
Version Model Number | 2100-230 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | 303-790-9411 |
info@sontecintsruments.com | |
Phone | 303-790-9411 |
info@sontecintsruments.com |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896010178 [Primary] |
HIBCC | B09921002300 [Primary] |
DXC | Clamp, Vascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B09921002300]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09921002300]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2018-08-24 |
BO9921002300 | COOLEY MULTI PURPOSE CLAMP ANGLED |
B09921002340 | COOLEY MULTI PURPOSE CLAMP ANGLED |
B09921002320 | COOLEY MULTI PURPOSE CLAMP ANGLED |
B09921002300 | COOLEY MULTI PURPOSE CLAMP ANGLED |