SecurAcath 400130

GUDID 10865382000201

INTERRAD MEDICAL, INC

Wearable percutaneous catheter/tube holder
Primary Device ID10865382000201
NIH Device Record Key6f7a6b3b-7a9b-4383-adb8-7f0db5fc39cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameSecurAcath
Version Model Number3F
Catalog Number400130
Company DUNS555472310
Company NameINTERRAD MEDICAL, INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Catheter Gauge3 French

Device Identifiers

Device Issuing AgencyDevice ID
GS100865382000204 [Primary]
GS110865382000201 [Package]
Contains: 00865382000204
Package: Shelf Box [10 Units]
In Commercial Distribution

FDA Product Code

OKCImplanted Subcutaneous Securement Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-07-22
Device Publish Date2016-09-15

On-Brand Devices [SecurAcath]

108653820002568F
108653820002497F
108653820002326F
108653820002255F
108653820002184F
108653820002013F
0086538200029710F
0086538200028012F

Trademark Results [SecurAcath]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SECURACATH
SECURACATH
85591187 4348913 Live/Registered
Interrad Medical, Inc.
2012-04-06
SECURACATH
SECURACATH
78703147 4071317 Live/Registered
Interrad Medical, Inc.
2005-08-30
SECURACATH
SECURACATH
74353255 1813589 Dead/Cancelled
HDC, Inc.
1993-01-28

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