CONVATEC 1712754

GUDID 24026704582390

Red Rubber 12FR Kit

TELEFLEX INCORPORATED

Indwelling urethral drainage catheter

• Primary Device ID: 24026704582390
• NIH Device Record Key: aecd500e-1097-4b4f-a42d-713de221c3d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONVATEC
• Version Model Number: IPN050245
• Catalog Number: 1712754
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• 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

Device Dimensions

• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch
• Height: 0.5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	14026704582393 [Primary]
GS1	24026704582390 [Package]; Contains: 14026704582393; Package: Box [100 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K010420

FDA Product Code

• KOD: CATHETER, UROLOGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2018-12-10
• Device Publish Date: 2016-09-16

On-Brand Devices [CONVATEC]

• 24026704582437: 14FR Female Kit
• 24026704582420: Red Rubber Tiemann 14FR Kit
• 24026704582413: Red Rubber 16FR Kit
• 24026704582406: Red Rubber 14FR Kit
• 24026704582390: Red Rubber 12FR Kit
• 24026704582383: Tiemann 16FR Kit
• 24026704582376: Tiemann 14FR Kit
• 24026704582369: Tiemann 12FR Kit
• 24026704582352: Soft 14FR Kit
• 24026704582345: Soft 12FR Kit