MICASEPT DEBAKEY PULMONALIS CLAMP 20919-35-024

GUDID 00192896008465

MICASEPT DEBAKEY PULMONALIS CLAMP WITH HEGAR RATCHET ANGLED DOWN CURVED LEFT

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00192896008465
NIH Device Record Key4245fe12-b028-4825-9cf9-18d2f0b20009
Commercial Distribution StatusIn Commercial Distribution
Brand NameMICASEPT DEBAKEY PULMONALIS CLAMP
Version Model Number20919-35-024
Catalog Number20919-35-024
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-821-7496
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
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0
Length300 Millimeter
Outer Diameter4.5 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896008465 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896008465]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-17
Device Publish Date2018-08-15

On-Brand Devices [MICASEPT DEBAKEY PULMONALIS CLAMP ]

B09920919350230MICASEPT DEBAKEY PULMONALIS CLAMP HEGAR RATCHET CURVED LEFT CURVED DOWN
00192896008465MICASEPT DEBAKEY PULMONALIS CLAMP WITH HEGAR RATCHET ANGLED DOWN CURVED LEFT
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