COOLIEF* Cooled Radiofrequency QUICKCLAMP* Device SIA-QC

GUDID 10680651124767

QUICHYHLAMPTM DEVICE

Avanos Medical, Inc.

Wearable percutaneous catheter/tube holder

• Primary Device ID: 10680651124767
• NIH Device Record Key: c90afbce-582e-444a-9d9e-b18acb908a10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COOLIEF* Cooled Radiofrequency QUICKCLAMP* Device
• Version Model Number: 12476
• Catalog Number: SIA-QC
• Company DUNS: 079375431
• Company Name: Avanos Medical, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx
• Phone: +1(844)425-9273
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10680651124767 [Primary]

FDA Product Code

• HXD: CLAMP

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-08-02
• Device Publish Date: 2016-05-17

Devices Manufactured by Avanos Medical, Inc.

• 10193494001695 - PROBLOC* II Insulated Regional Block Needle: 2025-12-16 PROBLOC* II Insulated Regional block Needle with Injection Set and Stimulation Cable
• 10193494001701 - PROBLOC* II Insulated Regional Block Needle: 2025-12-16 PROBLOC* II Insulated Regional block Needle with Injection Set and Stimulation Cable
• 10193494001718 - PROBLOC* II Insulated Regional Block Needle: 2025-12-16 PROBLOC* II Insulated Regional block Needle with Injection Set and Stimulation Cable
• 10193494001725 - PROBLOC* II Insulated Regional Block Needle: 2025-12-16 PROBLOC* II Insulated Regional block Needle with Injection Set and Stimulation Cable
• 10193494001732 - PROBLOC* II Insulated Regional block Needle: 2025-12-08 Probloc II Series
• 10193494001749 - PROBLOC* II Insulated Regional block Needle: 2025-12-08 Probloc II Series
• 10193494001756 - PROBLOC* II Insulated Regional block Needle: 2025-12-08 Probloc II Series
• 10193494001763 - PROBLOC* II Insulated Regional block Needle: 2025-12-08 Probloc II Series