Adjustable Depth Stop 317-0009

GUDID 00816950029400

Adjustable Depth Stop

SMV SCIENTIFIC LLC

Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable Surgical depth gauge, reusable
Primary Device ID00816950029400
NIH Device Record Key69b7047f-629a-43f1-8391-114f916bd208
Commercial Distribution StatusIn Commercial Distribution
Brand NameAdjustable Depth Stop
Version Model Number317-0009
Catalog Number317-0009
Company DUNS089645059
Company NameSMV SCIENTIFIC LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com
Phone1-800-969-0639
Emailquality@osteocentric.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816950029400 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


[00816950029400]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-17
Device Publish Date2021-05-07

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