Fox Converting

GUDID 20024562001231

FOX CONVERTING, INC.

Sterilization packaging, single-use

• Primary Device ID: 20024562001231
• NIH Device Record Key: 13820a69-08ec-4c7a-8640-fabfd4258144
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fox Converting
• Version Model Number: 150000123
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Cool & Dry Environment
• Special Storage Condition, Specify: Between 0 and 0 *Cool & Dry Environment

Device Identifiers

Device Issuing Agency	Device ID
GS1	00024562001237 [Unit of Use]
GS1	20024562001231 [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: 2017-06-21

On-Brand Devices [Fox Converting]

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