Primary Device ID | 00192896120747 |
NIH Device Record Key | 2390e8f6-db74-4a7a-83fc-cd6740e9ed3b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Canal Finder Raspatory |
Version Model Number | 345-221 |
Catalog Number | 345-221 |
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 | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
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 | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Length | 8 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896120747 [Primary] |
LXH | Orthopedic manual surgical instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
[00192896120747]
Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-04 |
Device Publish Date | 2024-10-25 |
00192896120747 | Canal Finder Raspatory With Silicone Handle Straight |
00192896120730 | Canal Finder Raspatory With Silicone Handle Curved |