Primary Device ID | 00192896117549 |
NIH Device Record Key | 43897a4d-c7e7-42d1-8440-cad88ca6831e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Debakey Retractor Frame |
Version Model Number | 2500-555 |
Catalog Number | 2500-555 |
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 | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896117549 [Primary] |
GAD | RETRACTOR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
[00192896117549]
Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-13 |
Device Publish Date | 2024-05-03 |
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00192896117914 - Fukushima Suction Tube | 2024-06-17 Fukushima Suction Tube Tapered Shaft Teardrop Finger Control |
00192896117921 - Fukushima Suction Tube | 2024-06-17 Fukushima Suction Tube Tapered Shaft Teardrop Finger Control |
00192896117938 - Fukushima Suction Tube | 2024-06-17 Fukushima Suction Tube Tapered Shaft Teardrop Finger Control |