MICASEPT PULMONALIS CLAMP

GUDID B09920919340

MICASEPT PULMONALIS CLAMP ROUND RATCHET CURVED RIGHT CURVED DOWN

SONTEC INSTRUMENTS, INC.

Rigid endoscopic grasping forceps, reusable 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 IDB09920919340
NIH Device Record Key3e2471da-17fa-4e41-95bf-db5e2c3c7328
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMICASEPT PULMONALIS CLAMP
Version Model Number20919-34
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

Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM

Device Dimensions

Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Length300 Millimeter
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB09920919340 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B09920919340]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2018-07-06
Device Publish Date2016-09-23

On-Brand Devices [MICASEPT PULMONALIS CLAMP ]

B09920919340040MICASEPT PULMONALIS CLAMP WITH HEGAR RATCHET CURVED RIGHT CURVED DOWN
B09920919350040MICASEPT PULMONALIS CLAMP HEGAR RATCHET CURVED LEFT CURVED DOWN
B09920919340MICASEPT PULMONALIS CLAMP ROUND RATCHET CURVED RIGHT CURVED DOWN
00192896115477Micasept Pulmonalis Clamp With Round Ratchet 30 Degrees Curved Down Right
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.