Schepens Scleral Depressor 10-3820

GUDID 00192896120273

Schepens Scleral Depressor With Thimble Large Size #12 Black

SONTEC INSTRUMENTS, INC.

Orbital depressor, reusable
Primary Device ID00192896120273
NIH Device Record Key55623ce8-ed33-4d8c-89bf-ee0459c39d10
Commercial Distribution StatusIn Commercial Distribution
Brand NameSchepens Scleral Depressor
Version Model Number10-3820
Catalog Number10-3820
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896120273 [Primary]

FDA Product Code

HNXDepressor, orbital

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

[00192896120273]

Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-23
Device Publish Date2024-10-15

On-Brand Devices [Schepens Scleral Depressor]

00192896099470SCHEPENS SCLERAL DEPRESSOR WITH THIMBLE SMALL SIZE #8 BLACK
00192896120273Schepens Scleral Depressor With Thimble Large Size #12 Black
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.