QUIKCLOT 4030

GUDID 20841495150221

TELEFLEX INCORPORATED

Non-organic haemostatic agent

• Primary Device ID: 20841495150221
• NIH Device Record Key: e615a19d-df0d-47b1-9812-ccd396f4c87f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: QUIKCLOT
• Version Model Number: IPN926808
• Catalog Number: 4030
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841495150224 [Primary]
GS1	20841495150221 [Package]; Contains: 10841495150224; Package: Box [10 Units]; In Commercial Distribution
GS1	30841495150228 [Package]; Package: Case [1 Units]; In Commercial Distribution

FDA Product Code

• POD: Temporary, internal use hemostatic

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: 2023-06-14
• Device Publish Date: 2023-06-06

On-Brand Devices [QUIKCLOT]

• 20841495150221: IPN926808
• 20841495150214: IPN926811
• 20841495150030: IPN921525
• 20841495150023: IPN926809
• 20841495150016: QuikClot Control+ Hemostatic Dressing 8" x 8" 2-Ply
• 20841495150252: QuikClot Combat Gauze
• 20841495150368: IPN928798
• 30841495150358: QuikClot Roll Hemostatic Dressing,CE,Multi-lg,10x
• 20841495150344: QuikClot Z-Fold Hemostatic Dressing,Mult-lang,CE,10x
• 20841495150290: QuikClot Hemostatic Dressing 2x2 ,CE,Multi-lang10x
• 30841495150242: QuikClot Interventional Pre-Slit w/ Tegaderm
• 30841495150235: QuikClot Interventional w/ Tegaderm
• 20841495150337: QuikClot Interventional, N/Clamshell, N/Tegaderm, Multi-Lang, 10X
• 20841495150306: QuikClot TraumaPad, CE,Multi-language, 10x
• 20841495150283: QuikClot Hemostatic Dressing 4x4 ,CE,Multi-lang10x