Mictec Fenestrated Grasping Forceps 20820-15

GUDID 00192896118201

Mictec Fenestrated Grasping Forceps Rhombic With Ratchet Parallel Shaft

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00192896118201
NIH Device Record Key8bb83920-5eb2-4099-967e-acb9ca1036fe
Commercial Distribution StatusIn Commercial Distribution
Brand NameMictec Fenestrated Grasping Forceps
Version Model Number20820-15
Catalog Number20820-15
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

Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter
Length360 Millimeter
Width10 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896118201 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

[00192896118201]

Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-11
Device Publish Date2024-07-03

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