FINISHING KIT N-71000P

GUDID D757N71000P1

BISCO INC.

Dental abrasive disk, reusable

• Primary Device ID: D757N71000P1
• NIH Device Record Key: b3d1132a-843d-47ba-8640-2e9f571425e3
• Commercial Distribution Discontinuation: 2018-12-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: FINISHING KIT
• Version Model Number: N-71000P
• Catalog Number: N-71000P
• Company DUNS: 053529939
• Company Name: BISCO INC.
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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(847)534-6000
• Email: sales@bisco.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D757N71000P1 [Primary]

FDA Product Code

• DZN: INSTRUMENTS, DENTAL HAND

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: 2020-03-23
• Device Publish Date: 2018-11-12

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