VIA procedure kit - custom 00717100

GUDID 10816765014780

The VIA Procedure Kit - custom includes transport pad, gauze pads, Via enzymatic sponge, Via basin, biohazard sticker, lubricating jelly, Double Header cleaning brush, BioGuard air water and suction valves, and solidifier.

US Endoscopy

Endoscopy preparation kit

• Primary Device ID: 10816765014780
• NIH Device Record Key: ca91996e-f21b-4146-a196-cd88441b7baa
• Commercial Distribution Discontinuation: 2020-02-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: VIA procedure kit - custom
• Version Model Number: 00717100
• Catalog Number: 00717100
• 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	00816765014783 [Primary]
GS1	10816765014780 [Package]; Contains: 00816765014783; Package: Box [20 Units]; Discontinued: 2020-02-03; Not in Commercial Distribution

FDA Product Code

• NWU: Endoscope introducer kit
• NWW: Hysteroscope accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-03
• Device Publish Date: 2018-07-17

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