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
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

Devices Manufactured by LACEY MANUFACTURING COMPANY, LLC

00853508002171 - BEST2023-06-23 Sheathed Bayonet Surgical Knife
00853508002188 - BEST2023-06-23 Sheathed Bayonet Surgical Knife
00853508002218 - BEST PAK Access Needle 2023-06-23 Pedicle Access Needle PAK Bevel/Bevel
00853508002225 - BEST PAK Access Needle 2023-06-23 PAK Access Needle Trocar/Trocar
00853508002232 - BEST PAK Access Needle 2023-06-23 PAK Pedicle Access Needle Trocar/Bevel
00853508002249 - BEST PAK Access Needle 2023-06-23 PAK Pedicle Access Needle XPAK Bevel
00853508002256 - BEST PAK Access Needle 2023-06-23 PAK Access Needle XPAK Trocar
00853508002263 - BEST2023-06-23 Sheathed Bayonet Surgical Knife
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.