ECS5330

GUDID 03700393301032

Single use, atraumatic Endoclinch forceps for laparoscopic surgery

PETERS SURGICAL

Rigid endoscopic tissue manipulation forceps, single-use
Primary Device ID03700393301032
NIH Device Record Key6ac96548-28b5-4aaa-a2f5-8486f7f111c2
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberECS5330
Catalog NumberECS5330
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
GS103700393301032 [Package]
Contains: 03700393301049
Package: Box [5 Units]
In Commercial Distribution
GS103700393301049 [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 Number5
Public Version Date2019-09-20
Device Publish Date2016-09-12

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03661522023419 - ADVANTIME2024-12-20
03661522023464 - ADVANTIME2024-12-20
03661522023471 - ADVANTIME2024-12-20
03661522023495 - ADVANTIME2024-12-20
03661522023501 - ADVANTIME2024-12-20

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