Vasto 00712810

GUDID 10724995184213

The Vasto Bite Block is used to protect the endoscope insertion tube from being bitten by the patient.

US Endoscopy

Endoscopic bite block, basic, single-use

• Primary Device ID: 10724995184213
• NIH Device Record Key: fa828d6f-a6e0-4af5-8abe-33a6984b01d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vasto
• Version Model Number: 00712810
• Catalog Number: 00712810
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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
• 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
• 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
• 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
• 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
• Phone: +1(800)548-4873
• Email: xx@xx.xx

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store at controlled room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995184216 [Primary]
GS1	10724995184213 [Package]; Contains: 00724995184216; Package: Case [100 Units]; In Commercial Distribution

FDA Product Code

• MNK: Endoscopic bite block

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-08
• Device Publish Date: 2021-03-31

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• 00724995244613 - Lumiflex: 2025-06-11 LUMIFLEX 3-STAGE Balloon Dilatation Catheter 5.5cm/8mm no wire is made of nylon and is a progressive stage balloon capable of th