Fox Converting

GUDID 20024562012046

FOX CONVERTING, INC.

Sterilization packaging, single-use

• Primary Device ID: 20024562012046
• NIH Device Record Key: 5d15c37c-8230-4841-8df8-8e4a53c6358f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fox Converting
• Version Model Number: 100001204
• Company DUNS: 006140123
• Company Name: FOX CONVERTING, INC.
• Device Count: 1000
• 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	00024562012042 [Unit of Use]
GS1	20024562012046 [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: 2017-02-06

On-Brand Devices [Fox Converting]

• 20024562502035: 150000203
• 20024562012084: 100001208
• 20024562012060: 100001206
• 20024562012053: 100001205
• 20024562012046: 100001204
• 20024562012039: 100001203
• 20024562001231: 150000123