MAXI LD 4171640S

GUDID 20705032002568

MAXI LD 7F 16X4 80CM

CORDIS CORPORATION

Peripheral angioplasty balloon catheter, basic
Primary Device ID20705032002568
NIH Device Record Keyd696bdb0-312d-4220-bdbc-140c6d56a40d
Commercial Distribution StatusIn Commercial Distribution
Brand NameMAXI LD
Version Model Number4171640S
Catalog Number4171640S
Company DUNS806136177
Company NameCORDIS 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged
Special Storage Condition, SpecifyBetween 0 and 0 *Store in cool, dark, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Do not use if package is damanged

Device Identifiers

Device Issuing AgencyDevice ID
GS120705032002568 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LITCatheter, angioplasty, peripheral, transluminal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-01

On-Brand Devices [MAXI LD]

20705032002728MAXI LD 7F 25X4 80CM
20705032002711MAXI LD 7F 25X4 110CM
20705032002704MAXI LD 7F 22X4 80CM
20705032002698MAXI LD 7F 22X4 110CM
20705032002667MAXI LD 7F 20X6 80CM
20705032002650MAXI LD 7F 20X6 110CM
20705032002643MAXI LD 7F 20X4 80CM
20705032002636MAXI LD 7F 20X4 110CM
20705032002629MAXI LD 7F 18X6 80CM
20705032002612MAXI LD 7F 18X6 110CM
20705032002605MAXI LD 7F 18X4 80CM
20705032002599MAXI LD 7F 18X4 110CM
20705032002582MAXI LD 16X6 80CM
20705032002575MAXI LD 7F 16X6 110CM
20705032002568MAXI LD 7F 16X4 80CM
20705032002551MAXI LD 7F 16X4 110CM
20705032002537MAXI LD 7F 15X6 80CM
20705032002520MAXI LD 7F 15X6 110CM
20705032002506MAXI LD 7F 15X4 80CM
20705032002490MAXI LD 7F 15X4 110CM
20705032002476MAXI LD 7F 15X2 80CM
20705032002469MAXI LD 7F 15X2 110CM
20705032002452MAXI LD 7F 14X6 80CM
20705032002445MAXI LD 7F 14X6 110CM
20705032002438MAXI LD 7F 14X4 80CM
20705032002421MAXI LD 7F 14X4 110CM
20705032002407MAXI LD 7F 25X4 80CM
20705032002391MAXI LD 7F 25X4 110CM
20705032002384MAXI LD 7F 22X4 80CM
20705032002377MAXI LD 7F 22X4 110CM
20705032002346MAXI LD 7F 20X8 80CM
20705032002339MAXI LD 7F 20X8 110CM
20705032002315MAXI LD 7F 20X6 80CM
20705032002308MAXI LD 7F 20X6 110CM
20705032002285MAXI LD 7F 20X4 80CM
20705032002278MAXI LD 7F 20X4 110CM
20705032002261MAXI LD 7F 18X6 80CM
20705032002247MAXI LD 7F 18X4 80CM
20705032002230MAXI LD 7F 18X4 110CM
20705032002223MAXI LD 7F 16X6 80CM
20705032002216MAXI LD 7F 16X6 110CM
20705032002209MAXI LD 7F 16X4 80CM
20705032002193MAXI LD 7F 16X4 110CM
20705032002179MAXI LD 7F 15X6 80CM
20705032002162MAXI LD 7F 15X6 110CM
20705032002148MAXI LD 7F 15X4 80CM
20705032002131MAXI LD 7F 15X4 110CM
20705032002117MAXI LD 7F 15X2 80CM
20705032002100MAXI LD 7F 15X2 110CM
20705032002094MAXI LD 7F 14X6 80CM

Trademark Results [MAXI LD]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MAXI LD
MAXI LD
76165721 2506462 Live/Registered
CARDINAL HEALTH 529, LLC
2000-11-16

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