Ritus 8888412305

GUDID 30884521803293

Preoperative Peritoneal Dialysis Catheter Stencil

Covidien LP

Peritoneal dialysis catheter introduction set Peritoneal dialysis catheter introduction set Peritoneal dialysis catheter introduction set Peritoneal dialysis catheter introduction set
Primary Device ID30884521803293
NIH Device Record Keyeba2f73e-decb-409d-9856-6854d081c03c
Commercial Distribution StatusIn Commercial Distribution
Brand NameRitus
Version Model Number8888412305
Catalog Number8888412305
Company DUNS058614483
Company NameCovidien LP
Device Count5
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521803299 [Primary]
GS110884521803299 [Primary]
GS110884521803299 [Primary]
GS110884521803299 [Primary]
GS130884521803293 [Unit of Use]
GS130884521803293 [Unit of Use]
GS130884521803293 [Unit of Use]
GS130884521803293 [Unit of Use]

FDA Product Code

KGZACCESSORIES, CATHETER
KGZACCESSORIES, CATHETER
KGZACCESSORIES, CATHETER
KGZACCESSORIES, CATHETER

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-21
Device Publish Date2020-05-13

Devices Manufactured by Covidien LP

10884521725942 - Emprint2020-05-25 Short Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521725959 - Emprint2020-05-25 Standard Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521725966 - Emprint2020-05-25 Long Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521806511 - Emprint2020-05-25 Short Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521806528 - Emprint2020-05-25 Standard Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521806535 - Emprint2020-05-25 Long Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone
10884521806542 - Emprint2020-05-25 Short Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone - Reinforced Antenna
10884521806559 - Emprint2020-05-25 Standard Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone - Reinforced Antenna

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.