Primary Device ID | 00192896101494 |
NIH Device Record Key | 0baf1819-6b7a-4dea-a27d-d7b2ac656643 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VATS SINGLEY TUTTLE LUNG GRASPING FORCEPS |
Version Model Number | 2100-822A |
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 |
Length | 13 Inch |
Device Size Text, specify | 0 |
Length | 13 Inch |
Device Size Text, specify | 0 |
Length | 13 Inch |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896101494 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896101494]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896101494]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896101494]
Dry Heat Sterilization;Moist Heat or Steam 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 |
00192896101494 | V.A.T.S. SINGLEY TUTTLE LUNG GRASPING FORCEPS STRAIGHT WITHOUT RATCHET |
00192896108424 | VATS Singley Tuttle Lung Grasping Forceps With Ratchet 6 Millimeters Straight Titanium |