ULTRAPRO UPPM1

GUDID 20705031085975

Polypropylene partially absorbable large blue / undyed Plug and Onlay Patch

Johnson & Johnson International Inc.

Extra-gynaecological surgical mesh, composite-polymer

• Primary Device ID: 20705031085975
• NIH Device Record Key: 64efac63-0187-408d-a10c-662ffbfd8e3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRAPRO
• Version Model Number: UPPM1
• Catalog Number: UPPM1
• Company DUNS: 372587696
• Company Name: Johnson & Johnson International Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx
• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx
• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx
• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx
• Phone: +1(877)384-4266
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705031085978 [Primary]
GS1	20705031085975 [Package]; Contains: 10705031085978; Package: BOX [1 Units]; In Commercial Distribution

FDA Product Code

• FTL: Mesh, surgical, polymeric

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-16
• Device Publish Date: 2022-11-08

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