HIGH PRESSURE TUBING VGPMT0501

GUDID 00850004162064

VGPMT0501 HIGH PRESSURE TUBING (30cm)

VALFLUX GROUP, LLC

Arterial blood pressure catheter

• Primary Device ID: 00850004162064
• NIH Device Record Key: f39a8eae-730b-4c1e-87b7-2eed41f38cef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HIGH PRESSURE TUBING
• Version Model Number: VGPMT0501
• Catalog Number: VGPMT0501
• Company DUNS: 050193715
• Company Name: VALFLUX GROUP, LLC
• 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: false
• 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

Customer Support Contacts

• Phone: +556230916442
• Email: regulacao@valflux.com.br

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850004162064 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170014

FDA Product Code

• DXT: INJECTOR AND SYRINGE, ANGIOGRAPHIC

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: 2019-01-18
• Device Publish Date: 2018-12-18

On-Brand Devices [HIGH PRESSURE TUBING]

• 00850004162118: VGPMT0509 HIGH PRESSURE TUBING (180cm)
• 00850004162101: VGPMT0505 HIGH PRESSURE TUBING (150cm)
• 00850004162095: VGPMT0504 HIGH PRESSURE TUBING (120cm)
• 00850004162088: VGPMT0503 HIGH PRESSURE TUBING (90cm)
• 00850004162071: VGPMT0502 HIGH PRESSURE TUBING (60cm)
• 00850004162064: VGPMT0501 HIGH PRESSURE TUBING (30cm)