MD5330

GUDID 03700393300844

Single use, Maryland dissector 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 ID03700393300844
NIH Device Record Key3adc0ed9-f325-4bcf-84db-23d3a1b5deb5
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberMD5330
Catalog NumberMD5330
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

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
Length330 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103700393300844 [Package]
Contains: 03700393300899
Package: Box [5 Units]
In Commercial Distribution
GS103700393300899 [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 StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-20
Device Publish Date2016-09-12

Devices Manufactured by PETERS SURGICAL

03661522100882 - Applier, hemostatic clip2024-01-10
03661522100899 - Applier, hemostatic clip2024-01-10
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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.