620-010-101

GUDID 07613327063189

Veress Needle

STRYKER CORPORATION

Spring-loaded pneumoperitoneum needle, reusable
Primary Device ID07613327063189
NIH Device Record Key1d0131b4-2fb2-4719-9f19-a172e7b5de70
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0620010101
Catalog Number620-010-101
Company DUNS187502109
Company NameSTRYKER CORPORATION
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)624-4422
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327063189 [Primary]

FDA Product Code

HIGINSUFFLATOR, HYSTEROSCOPIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327063189]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

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