BIOPSY FORCEPS STD 504302L

GUDID 20705032056127

BIOPSY FORCEPS 7F 50CM

CORDIS CORPORATION

Endomyocardial biopsy forceps, single-use
Primary Device ID20705032056127
NIH Device Record Key96d61a9e-8316-4467-b406-cf0e8f9a02c8
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIOPSY FORCEPS STD
Version Model Number504302L
Catalog Number504302L
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110705032056120 [Primary]
GS120705032056127 [Package]
Contains: 10705032056120
Package: Box [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWZDEVICE, BIOPSY, ENDOMYOCARDIAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-04
Device Publish Date2024-02-23

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20705032057575 - Palmaz Genesis2024-08-08 STENT GENESIS 39MM PERIPHERAL
20705032057612 - Palmaz Genesis2024-08-08 STENT GENESIS 59MM PERIPHERAL
20705032062029 - PALMAZ BLUE2024-08-08 Blue/AviatorPlus 5x12/80P PKG
20705032062258 - PALMAZ BLUE2024-08-08 Blue/AviatorPlus 5x24/80P PKG

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