Henry Schein

GUDID 20024562016860

FOX CONVERTING, INC.

Sterilization packaging, single-use

• Primary Device ID: 20024562016860
• NIH Device Record Key: f09f75ff-10b5-4155-81e6-403dd01ed12d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Henry Schein
• Version Model Number: 160001686
• Company DUNS: 006140123
• Company Name: FOX CONVERTING, INC.
• Device Count: 5000
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00024562016863 [Unit of Use]
GS1	20024562016860 [Primary]

FDA Product Code

• FRG: Wrap, Sterilization

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-11-02

On-Brand Devices [Henry Schein]

• 20024562016860: 160001686
• 20024562001668: 160000166
• 10024562016863: 160001686
• 10024562001661: 160000166