5053

GUDID 03700393300172

Single use, sharp trocar for laparoscopic surgery

PETERS SURGICAL

Laparoscopic access cannula, single-use
Primary Device ID03700393300172
NIH Device Record Key2d5b76a0-68da-4660-b574-5884e27507c6
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5053
Catalog Number5053
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+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
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS103700393300172 [Package]
Contains: 03700393300189
Package: Box [25 Units]
In Commercial Distribution
GS103700393300189 [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 Number6
Public Version Date2020-01-09
Device Publish Date2016-09-12

Devices Manufactured by PETERS SURGICAL

03661522023228 - ADVANTIME2024-12-20
03661522023389 - ADVANTIME2024-12-20
03661522023402 - ADVANTIME2024-12-20
03661522023419 - ADVANTIME2024-12-20
03661522023464 - ADVANTIME2024-12-20
03661522023471 - ADVANTIME2024-12-20
03661522023495 - ADVANTIME2024-12-20
03661522023501 - ADVANTIME2024-12-20

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