HK Non-Sterile Super Absorbent Pads XL PD-XL

GUDID 00816989021093

HK Non-Sterile Super Absorbent Pads XL

HK SURGICAL INC.

Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad Absorbent wound compression pad

• Primary Device ID: 00816989021093
• NIH Device Record Key: 5bf8bf1a-0649-441a-b3da-e06e3da66a02
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HK Non-Sterile Super Absorbent Pads XL
• Version Model Number: PD-XL
• Catalog Number: PD-XL
• Company DUNS: 106885259
• Company Name: HK SURGICAL INC.
• Device Count: 48
• 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: 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: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com
• Phone: 949-369-0101
• Email: hkinfo@hksurgical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816989021093 [Primary]
GS1	10816989021090 [Unit of Use]

FDA Product Code

• FRL: Fiber, Medical, Absorbent

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-09
• Device Publish Date: 2021-07-31

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