Metzenbaum Soft Preparation Scissors 2901-304

GUDID 00192896120150

Metzenbaum Soft Preparation Scissors Curved Double Action Jaws

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable
Primary Device ID00192896120150
NIH Device Record Key8cbe3fe8-9271-4eb9-83a4-c2c9e0356214
Commercial Distribution StatusIn Commercial Distribution
Brand NameMetzenbaum Soft Preparation Scissors
Version Model Number2901-304
Catalog Number2901-304
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
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 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 Dimensions

Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter
Device Size Text, specify0
Length360 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896120150 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

Dry Heat Sterilization

[00192896120150]

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

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