Micasept Pulmonalis Clamp 20919-34

GUDID 00192896115477

Micasept Pulmonalis Clamp With Round Ratchet 30 Degrees Curved Down Right

SONTEC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable
Primary Device ID00192896115477
NIH Device Record Keya5894b74-3872-4d23-9977-cce650419881
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicasept Pulmonalis Clamp
Version Model Number20919-34
Catalog 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 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

Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter
Length300 Millimeter
Lumen/Inner Diameter4.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896115477 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115477]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-29
Device Publish Date2023-08-21

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.