VIA procedure kit - custom 00717089

GUDID 10816765014704

The VIA Procedure Kit - custom includes transport pad, basin, Via enzymatic sponge, biohazard sticker, lubricating jelly, DuoSwift combination squeegee brush, and BioGuard air/water and suction valves.

US Endoscopy

Endoscopy preparation kit

• Primary Device ID: 10816765014704
• NIH Device Record Key: 497477b0-7196-4d44-b896-deadf002438e
• Commercial Distribution Discontinuation: 2020-01-16
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: VIA procedure kit - custom
• Version Model Number: 00717089
• Catalog Number: 00717089
• Company DUNS: 627879687
• Company Name: US Endoscopy
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816765014707 [Primary]
GS1	10816765014704 [Package]; Contains: 00816765014707; Package: Box [20 Units]; Discontinued: 2020-01-16; Not in Commercial Distribution

FDA Product Code

• NWU: Endoscope introducer kit

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: 2020-01-17
• Device Publish Date: 2018-07-17

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