HIGHFLOW 527787

GUDID 10705032011143

CATH F7 HF MP A2 125CM 2SH

CORDIS CORPORATION

Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use

• Primary Device ID: 10705032011143
• NIH Device Record Key: 81dfbb78-2d65-4398-9c3a-b39bad5e12c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HIGHFLOW
• Version Model Number: 527787
• Catalog Number: 527787
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• 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: false
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705032011143 [Primary]
GS1	20705032011140 [Package]; Package: BOX [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K862006

FDA Product Code

• DQO: CATHETER, INTRAVASCULAR, DIAGNOSTIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-02-15
• Device Publish Date: 2017-09-18

On-Brand Devices [HIGHFLOW]

• 10705032011068: CATH F7 HF IM 100CM
• 10705032011020: CATH F7 HF PIG 145 110CM 6SH
• 10705032010986: CATH F7 HF PIG 110CM 8SH
• 10705032010962: CATH F7 HF AR MOD 100CM
• 10705032010955: CATH F7 HF N.I.H. 100CM 4SH
• 10705032010924: CATH F7 HF AL II 100CM
• 10705032010917: CATH F7 HF AL I 100CM
• 10705032010863: CATH F7 HF JL 6 100CM
• 10705032010856: CATH F7 HF JR 5 100CM
• 10705032010849: CATH F7 HF JL 5 100CM
• 10705032010832: CATH F7 HF JR4 100CM
• 10705032010801: CATH F7 HF JL 3.5 100CM
• 10705032011143: CATH F7 HF MP A2 125CM 2SH
• 10705032011112: CATH F7 HF MPA1 100CM
• 10705032011082: CATH F7 HF LCB 100CM
• 10705032011075: CATH F7 HF RCB 100CM
• 10705032011037: CATH F7 HF PIG 155 110CM 12SH
• 10705032010979: CATH F7 HF PIG 110CM 12SH
• 10705032010931: CATH F7 HF MP A2 100CM 2SH
• 10705032010825: CATH F7 HF JL 4 100CM
• 10705032010818: CATH F7 HF JR 3.5 100CM