Primary Device ID | 10801741218078 |
NIH Device Record Key | a650f9b0-b903-4fb2-9d66-8af26b824688 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuCath Ace |
Version Model Number | AC1202250X |
Catalog Number | AC1202250X |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Size Text, specify | 0 |
Length | 2.25 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741218071 [Primary] |
GS1 | 10801741218078 [Package] Contains: 00801741218071 Package: CA [10 Units] In Commercial Distribution |
GS1 | 20801741218075 [Package] Package: BX [2 Units] In Commercial Distribution |
FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-21 |
Device Publish Date | 2021-10-13 |
20801741137956 | AccuCath ACE 20G 2.25”, Basic Kit |
20801741137949 | AccuCath ACE 18G 2.25”, Basic Kit |
10801741137935 | AccuCath ACE 22G 1.25”, Basic Kit |
10801741137928 | AccuCath ACE 20G 1.25”, Basic Kit |
10801741137911 | AccuCath ACE 18G 1.25”, Basic Kit |
10801741138017 | AccuCath ACE 20G 2.25”, Intermediate Kit |
10801741138000 | AccuCath ACE 18G 2.25”, Intermediate Kit |
10801741137997 | AccuCath ACE 22G 1.25”, Intermediate Kit |
10801741137973 | AccuCath ACE 18G 1.25”, Intermediate Kit |
10801741137980 | AccuCath ACE 20G 1.25”, Intermediate Kit |
10801741223690 | Catheter Placement Kit |
10801741218085 | AccuCath ACE with CUE 20G 2.25”, Intermediate Kit |
10801741218078 | AccuCath ACE with CUE 20G 2.25”, Basic Kit |
10801741218061 | AccuCath ACE with CUE 18G 2.25”, Intermediate Kit |
20801741218051 | AccuCath ACE with CUE 18G 2.25”, Basic Kit |
10801741226844 | Catheter Placement Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCUCATH ACE 87354572 5746076 Live/Registered |
Vascular Pathways, Inc. 2017-03-01 |