CAB3000

GUDID 03700393300318

single use, monopolar cable

PETERS SURGICAL

Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use Electrical-only medical device connection cable, single-use
Primary Device ID03700393300318
NIH Device Record Keyecb838f7-6387-478f-99a6-23539ced4a88
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberCAB3000
Catalog NumberCAB3000
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 Identifiers

Device Issuing AgencyDevice ID
GS103700393300318 [Package]
Contains: 03700393300325
Package: Box [25 Units]
In Commercial Distribution
GS103700393300325 [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

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

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