AccuCath Ace AC1202252X

GUDID 10801741218085

AccuCath ACE with CUE 20G 2.25”, Intermediate Kit

Bard Access Systems, Inc.

Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter
Primary Device ID10801741218085
NIH Device Record Key6aea5301-3540-4f2f-8ca8-cbd5edd209ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameAccuCath Ace
Version Model NumberAC1202252X
Catalog NumberAC1202252X
Company DUNS044611812
Company NameBard Access Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Producttrue
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

Customer Support Contacts

Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com

Device Dimensions

Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch
Device Size Text, specify0
Length2.25 Inch

Operating and Storage Conditions

Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741218088 [Primary]
GS110801741218085 [Package]
Contains: 00801741218088
Package: CA [10 Units]
In Commercial Distribution

FDA Product Code

FOZCatheter, intravascular, therapeutic, short-term less than 30 days

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-10-21
Device Publish Date2021-10-13

On-Brand Devices [AccuCath Ace]

20801741137956AccuCath ACE 20G 2.25”, Basic Kit
20801741137949AccuCath ACE 18G 2.25”, Basic Kit
10801741137935AccuCath ACE 22G 1.25”, Basic Kit
10801741137928AccuCath ACE 20G 1.25”, Basic Kit
10801741137911AccuCath ACE 18G 1.25”, Basic Kit
10801741138017AccuCath ACE 20G 2.25”, Intermediate Kit
10801741138000AccuCath ACE 18G 2.25”, Intermediate Kit
10801741137997AccuCath ACE 22G 1.25”, Intermediate Kit
10801741137973AccuCath ACE 18G 1.25”, Intermediate Kit
10801741137980AccuCath ACE 20G 1.25”, Intermediate Kit
10801741223690Catheter Placement Kit
10801741218085AccuCath ACE with CUE 20G 2.25”, Intermediate Kit
10801741218078AccuCath ACE with CUE 20G 2.25”, Basic Kit
10801741218061AccuCath ACE with CUE 18G 2.25”, Intermediate Kit
20801741218051AccuCath ACE with CUE 18G 2.25”, Basic Kit
10801741226844Catheter Placement Kit

Trademark Results [AccuCath Ace]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACCUCATH ACE
ACCUCATH ACE
87354572 5746076 Live/Registered
Vascular Pathways, Inc.
2017-03-01

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