Artisential Monopolar Hook

GUDID 08800042700638

Sterile Single-use Surgical Instrument used with electrosurgical generator intended to be used during laparoscopic procedure for manipulation of tissue to cauterize and dissect tissue.

LIVSMED

Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use
Primary Device ID08800042700638
NIH Device Record Key5b1a1555-9223-4a14-8ff0-b7c2bf594078
Commercial Distribution StatusIn Commercial Distribution
Brand NameArtisential Monopolar Hook
Version Model NumberAMHU01S-L
Company DUNS688360116
Company NameLIVSMED
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter
Shaft Length25 Centimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS108800042700638 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-01-30
Device Publish Date2024-01-22

On-Brand Devices [Artisential Monopolar Hook]

08800042700744Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700737Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700713Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700553Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700546Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700720Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700645Sterile Single-use Electrosurgical Instrument used for cutting and coagulation during laparoscop
08800042700676Sterile Single-use Surgical Instrument used with electrosurgical generator intended to be used d
08800042700669Sterile Single-use Surgical Instrument used with electrosurgical generator intended to be used d
08800042700621Sterile Single-use Surgical Instrument used with electrosurgical generator intended to be used d
08800042700638Sterile Single-use Surgical Instrument used with electrosurgical generator intended to be used d

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