ARROW PW-16130-HN

GUDID 20801902156710

ARROW(R) Marked Guidewire Hydrophilic-Coated Nitinol

TELEFLEX INCORPORATED

Peripheral vascular guidewire, manual

• Primary Device ID: 20801902156710
• NIH Device Record Key: b915a99b-9250-43d4-b5fb-e962d8164859
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARROW
• Version Model Number: IPN035907
• Catalog Number: PW-16130-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

Customer Support Contacts

• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	10801902156713 [Primary]
GS1	20801902156710 [Package]; Contains: 30801902156717; Package: Case [1 Units]; In Commercial Distribution
GS1	30801902156717 [Package]; Contains: 10801902156713; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070150

FDA Product Code

• DQX: Wire, guide, catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-27
• Device Publish Date: 2019-11-19

On-Brand Devices [ARROW]

• 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