CODMAN SOFWIRE 464010

GUDID 10705034002224

CODMAN SOF'WIRE Instrument Kit

Cerenovus, Inc.

Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Bone nail guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable
Primary Device ID10705034002224
NIH Device Record Key4df85fff-7ce3-4fe8-93b1-f2a40733bebf
Commercial Distribution Discontinuation2018-06-20
Commercial Distribution StatusNot in Commercial Distribution
Brand NameCODMAN SOFWIRE
Version Model Number464010
Catalog Number464010
Company DUNS607846297
Company NameCerenovus, Inc.
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 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(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034002224 [Primary]

FDA Product Code

HAOINSTRUMENT, SURGICAL, NON-POWERED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


[10705034002224]

Ethylene Oxide;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2023-09-15
Device Publish Date2016-12-31

On-Brand Devices [CODMAN SOFWIRE]

10705034002286CODMAN SOFWIRE SS Ti Single Cable with Leader, 1 Cinch, 1 Tightener
10705034002262CODMAN SOFWIRE SS Single Cable with Leader, 1 Cinch, 1 Tightener
10705034002224CODMAN SOF'WIRE Instrument Kit

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.