STRADIS HEALTHCARE

GUDID M752686176R11

CUSTOM SURGICAL KIT

STRADIS MEDICAL, LLC

General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated
Primary Device IDM752686176R11
NIH Device Record Keyb41c508f-bc76-4539-b12c-5df7637c25d0
Commercial Distribution Discontinuation2022-11-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSTRADIS HEALTHCARE
Version Model Number686-176 R1
Company DUNS174262477
Company NameSTRADIS MEDICAL, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM
Phone770-962-2425
EmailSALES@STRADISHEALTHCARE.COM

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM752686176R10 [Primary]
HIBCCM752686176R11 [Package]
Contains: M752686176R10
Package: case [5 Units]
Discontinued: 2022-11-30
Not in Commercial Distribution

FDA Product Code

OEZCardiovascular Procedure Kit

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-12-01
Device Publish Date2022-06-03

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