A5330

GUDID 03700393300561

Single use, atraumatic forceps with monopolar cautery for laparoscopic surgery

PETERS SURGICAL

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 Endoscopic electrosurgical electrode, monopolar, single-use
Primary Device ID03700393300561
NIH Device Record Key1ad1853c-6dcb-4a65-92dd-7810e1c3ff53
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberA5330
Catalog NumberA5330
Company DUNS265741780
Company NamePETERS SURGICAL
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

Phone+33470584170
Emailvectec@vectec.fr
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com

Device Dimensions

Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103700393300103 [Primary]
GS103700393300561 [Package]
Contains: 03700393300103
Package: Box [5 Units]
In Commercial Distribution

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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-20
Device Publish Date2016-09-12

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03661522100905 - Applier, hemostatic clip2024-01-10
03661522100929 - Applier, hemostatic clip2024-01-10
03661522100936 - Applier, hemostatic clip2024-01-10
03661522100912 - Applier, hemostatic clip2024-01-05
03661522000984 - Sertilac2023-06-19
03661522039540 - Applier, hemostatic clip2023-06-16

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