PRONTO 5040

GUDID 30841156100333

Pronto 035, 10F

TELEFLEX INCORPORATED

Thrombectomy suction catheter

• Primary Device ID: 30841156100333
• NIH Device Record Key: b12e0647-96a6-4d1e-a72b-cca732fa38b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRONTO
• Version Model Number: IPN913541
• Catalog Number: 5040
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• 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: false
• 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

Device Dimensions

• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French
• Catheter Gauge: 10 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156100339 [Primary]
GS1	30841156100333 [Package]; Contains: 10841156100339; Package: Box [1 Units]; In Commercial Distribution

FDA Product Code

• DXE: Catheter, embolectomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-11
• Device Publish Date: 2019-01-22

On-Brand Devices [PRONTO]

• 30841156100333: Pronto 035, 10F
• 20841156109001: PRONTO LP 5F
• 20841156108998: PRONTO LP 6F
• 20841156108981: PRONTO V4 6F
• 20841156108974: PRONTO V4 5.5F
• 20841156108967: PRONTO V3 6F
• 30841156100326: Pronto LP, 5F
• 30841156100319: Pronto LP, 6F
• 30841156100302: Pronto V3, 6F
• 30841156100258: Pronto V4, 8F
• 30841156100241: Pronto V4, 7F
• 30841156100234: Pronto V4, 6F
• 30841156100227: Pronto V4, 5.5F