Primary Device ID | 00192896121218 |
NIH Device Record Key | 8f406a2e-e745-4ff1-b281-58001f97d206 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Semken Tissue Forceps |
Version Model Number | 140-362 |
Catalog Number | 140-362 |
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 | 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 | 6.25 Inch |
Length | 6.25 Inch |
Length | 6.25 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896121218 [Primary] |
HTD | FORCEPS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896121218]
Dry Heat Sterilization
[00192896121218]
Dry Heat Sterilization
[00192896121218]
Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-04 |
Device Publish Date | 2025-02-24 |
00192896076501 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
00192896076495 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
00192896076471 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
00192896076464 | SEMKEN TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLATFORM |
00192896076297 | SEMKEN TISSUE FORCEPS DELICATE TIP |
00192896023222 | SEMKEN TISSUE FORCEPS |
00192896023215 | SEMKEN TISSUE FORCEPS |
00192896121218 | Semken Tissue Forceps With Tungsten Carbide Serrated Platform 1x2 Teeth |