Primary Device ID | 20801902156727 |
NIH Device Record Key | e70e5842-a3f0-4851-a714-7ce40bfcd9de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARROW |
Version Model Number | IPN035908 |
Catalog Number | PW-18080-HN |
Company DUNS | 002348191 |
Company Name | TELEFLEX INCORPORATED |
Device Count | 1 |
DM Exempt | true |
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 |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM | |
Phone | +1(919)544-8000 |
CS@TELEFLEX.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10801902156720 [Primary] |
GS1 | 20801902156727 [Package] Contains: 30801902156724 Package: Case [1 Units] In Commercial Distribution |
GS1 | 30801902156724 [Package] Contains: 10801902156720 Package: Box [5 Units] In Commercial Distribution |
DQX | Wire, guide, catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2019-11-19 |
00801902136749 | RediGuard IAB: 7Fr 30cc |
00801902136732 | RediGuard IAB: 8Fr 40cc |
00801902136725 | FiberOptix Ultra 8 IAB: 8Fr 30cc |
00801902136718 | FiberOptix Ultra 8 IAB: 8Fr 40cc |
00801902136701 | UltraFlex IAB: 7.5Fr 30cc |
00801902136695 | UltraFlex IAB: 7.5Fr 40cc |
30801902111549 | Arrow(R) Access Kit for use with 5 Fr. Peripherally Inserted Central Venous Catheter |
30801902111532 | Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter |
30801902111525 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902111471 | Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter |
30801902111464 | Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Inserted Central Venous Catheter |
30801902111457 | Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology |
30801902111440 | Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology |
30801902111433 | Peritoneal Lavage Kit |
30801902111426 | Maximal Barrier Drape |
30801902111402 | Arrow-Howes(TM) Quad-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWg+ard Bl |
30801902111365 | Arrowg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheter |
30801902111334 | Pressure Injectable ARROWg+ard Blue Plus(R) Multi-Lumen Central Venous Catheterization Kit |
30801902111327 | Arterial Catheterization Kit |
30801902111310 | Radial Artery Catheterization Kit |
30801902111303 | Arterial Catheterization Kit |
30801902109591 | Pressure Injectable ARROWg+ard Blue Plus(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109584 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109577 | Pressure Injectable ARROWg+ard Blue PLUS(R) Quad-Lumen Central Venous Catheterization Kit |
10801902109559 | NextStep(R) Antegrade Hemodialysis Catheterization Set Long-Term Access. Catheter Length, Tip to |
30801902109546 | Edge(R) Hemodialysis Catheterization Set Long-Term Access Catheter Length, Cuff to Tip: 31 cm |
30801902109539 | Spring Wire Guide Kit |
30801902109522 | Arterial Line Kit |
30801902109515 | Arterial Catheterization Kit |
10801902109504 | 15 Fr. x 19 cm NextStep(R) Antegrade Hemodialysis Catheterization Set, Long-Term Access Catheter |
30801902109485 | Pressure Injectable ARROWg+ard Blue Plus(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109478 | Arterial Line Kit with Sharps Safety Features |
30801902109461 | ARROWg+ard Blue(R) PSI Kit for use with 7.5 - 8 Fr. Catheters |
30801902109454 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109447 | Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit |
30801902109430 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109423 | ARROWg+ard Blue(R) Percutaneous Sheath Introducer Kit for use with 7.5 - 8 Fr. Catheter |
30801902109416 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902109409 | Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit |
30801902109218 | Percutaneous Sheath Introducer Kit for use with 7.5 - 8 Fr. Catheters |
30801902108464 | Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902108419 | Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902108396 | Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902108358 | Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902108327 | Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902106668 | Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit |
30801902105456 | Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902105449 | Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902105401 | Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
30801902105333 | Multi-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARROW 98785439 not registered Live/Pending |
Quad-States Industries, Inc. 2024-10-04 |
ARROW 98784387 not registered Live/Pending |
Quad-States Industries, Inc. 2024-10-03 |
ARROW 98699043 not registered Live/Pending |
Tatom, David 2024-08-14 |
ARROW 98415956 not registered Live/Pending |
Arrow Investment Analytics, LLC 2024-02-22 |
ARROW 98408806 not registered Live/Pending |
Southern California Regional Rail Authority ("SCRRA") 2024-02-16 |
ARROW 98387940 not registered Live/Pending |
ARROW FASTENER CO.,LLC 2024-02-02 |
ARROW 98235609 not registered Live/Pending |
Arrow Interactive LLC 2023-10-23 |
ARROW 98207717 not registered Live/Pending |
Maison Battat, Inc. 2023-10-03 |
ARROW 98109825 not registered Live/Pending |
ASSA ABLOY Access and Egress Hardware Group, Inc. 2023-07-31 |
ARROW 98109821 not registered Live/Pending |
ASSA ABLOY Access and Egress Hardware Group, Inc. 2023-07-31 |
ARROW 98109533 not registered Live/Pending |
ASSA ABLOY Access and Egress Hardware Group, Inc. 2023-07-31 |
ARROW 97926781 not registered Live/Pending |
Blake Bigot 2023-05-09 |