CAPIO 833-113

GUDID 24026704603866

Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle BSC

TELEFLEX INCORPORATED

Polyester suture, non-bioabsorbable, multifilament

• Primary Device ID: 24026704603866
• NIH Device Record Key: 0cf1da05-4ce8-4efb-a0cd-b60e926669b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIO
• Version Model Number: IPN000858
• Catalog Number: 833-113
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04026704603862 [Primary]
GS1	24026704603866 [Package]; Contains: 04026704603862; Package: Box [12 Units]; Discontinued: 2019-01-15; Not in Commercial Distribution

FDA Product Code

• GAT: SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-02-05
• Device Publish Date: 2015-10-16

On-Brand Devices [CAPIO]

• 34026704603894: Polypropylene Blue Monofilament Size 0 36" TC-43 Needle T Needle BSC
• 34026704603887: Polypropylene Blue Monofilament Size 0 48" TC-43 Needle BSC
• 34026704603870: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle T Needle BSC
• 34026704603863: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle BSC
• 24026704603897: Polypropylene Blue Monofilament Size 0 36" TC-43 Needle T Needle BSC
• 24026704603880: Polypropylene Blue Monofilament Size 0 48" TC-43 Needle BSC
• 24026704603873: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle T Needle BSC
• 24026704603866: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle BSC
• 24026704713510: Polypropylene Blue Monofilament Size 0 36" TC-43 Needle T Needle BSC
• 24026704713503: Polypropylene Blue Monofilament Size 0 48" TC-43 Needle BSC
• 24026704713497: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle T Needle BSC
• 24026704713480: Braided Polyester Green PTFE Impregnated Size 0 48" TC-43 Needle BSC