00712803

GUDID 10724995184152

The Bite Block Standard Adult, Velcro Strap is used to protect the endoscope insertion tube from being bitten by the patient.

US Endoscopy

Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use Endoscopic bite block, basic, single-use

• Primary Device ID: 10724995184152
• NIH Device Record Key: 3fe146ff-38ed-4c63-8650-9139ba2050bf
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 00712803
• Catalog Number: 00712803
• 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	00724995184155 [Primary]
GS1	10724995184152 [Package]; Contains: 00724995184155; 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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