NEIVERT HOOK RETRACTOR 199-408

GUDID 00192896098237

NEIVERT HOOK RETRACTOR

SONTEC INSTRUMENTS, INC.

Soft-tissue surgical hook, reusable
Primary Device ID00192896098237
NIH Device Record Key11b30936-2f35-4f05-9fdd-013f58fb415a
Commercial Distribution StatusIn Commercial Distribution
Brand NameNEIVERT HOOK RETRACTOR
Version Model Number199-408
Catalog Number199-408
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

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch
Length8 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896098237 [Primary]

FDA Product Code

GDGHook, Surgical, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896098237]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-07-19
Device Publish Date2019-07-11

On-Brand Devices [NEIVERT HOOK RETRACTOR]

00192896024397NEIVERT HOOK RETRACTOR DOUBLE ENDED
00192896098237NEIVERT HOOK RETRACTOR

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