BE-ST Bipolar Forceps Straight 1590-07

GUDID 00853508002119

Bayonet Bipolar Forceps Straight Tip

LACEY MANUFACTURING COMPANY, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use
Primary Device ID00853508002119
NIH Device Record Key0045fccc-582d-4fc1-a143-da0511dfb797
Commercial Distribution StatusIn Commercial Distribution
Brand NameBE-ST Bipolar Forceps Straight
Version Model Number1590-07
Catalog Number1590-07
Company DUNS958212029
Company NameLACEY MANUFACTURING COMPANY, LLC
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com
Phone2033367453
Emailjim.rogers@nninc.com

Device Dimensions

Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch
Length11.6 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100853508002119 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

[00853508002119]

Radiation Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-04-23
Device Publish Date2018-08-28

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