ZCG Metal Procelain

GUDID 06973133310183

It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full veneers and partial veneers.

BAOT Biological Technology Co., Ltd.

Dental appliance fabrication material, ceramic

• Primary Device ID: 06973133310183
• NIH Device Record Key: 768f14a4-afb6-4c7d-a4df-a25d27c59232
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ZCG Metal Procelain
• Version Model Number: Dentine A2
• Company DUNS: 560453518
• Company Name: BAOT Biological Technology Co., Ltd.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06973133310183 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182350

FDA Product Code

• EIH: Powder, Porcelain

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: 2020-05-22
• Device Publish Date: 2020-05-14

On-Brand Devices [ZCG Metal Procelain]

• 06973133310183: It is indicated for use for metal-ceramic full veneers and partial veneers and for zirconia full
• 06973133310244: Dental Ceramic is indicated for use for metal-ceramic full veneers and partial veneers and for z