Primary Device ID | 00192896101531 |
NIH Device Record Key | f9aabfb1-d3d6-43da-a9b6-80aa8e7fe983 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VATS FOERSTER CLAMP |
Version Model Number | 2100-8238A |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com |
Device Size Text, specify | 0 |
Length | 13 Inch |
Device Size Text, specify | 0 |
Length | 13 Inch |
Device Size Text, specify | 0 |
Length | 13 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896101531 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896101531]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896101531]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
[00192896101531]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2020-05-11 |
B0992100826A0 | VATS FOERSTER CLAMP WITHOUT RATCHET OVAL RING JAW CURVED LEFT |
B0992100824A0 | VATS FOERSTER CLAMP WITHOUT RATCHET OVAL RING JAW CURVED LEFT |
B09921008238A0 | VATS FOERSTER CLAMP WITHOUT RATCHET OVAL RING JAW CURVED LEFT |
00192896101531 | V.A.T.S. FOERSTER CLAMP CURVED LEFT WITHOUT RATCHET |