Gutta Percha F1/F2/F3

GUDID 08806387805465

Gutta Percha Points and Bars, Aurum Pro F1/F2/F3, 60 Points, P 71

Meta Biomed Co., Ltd.

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• Primary Device ID: 08806387805465
• NIH Device Record Key: eb3aa797-30b9-4b41-a9d7-cb47fda81271
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gutta Percha F1/F2/F3
• Version Model Number: 0546
• Company DUNS: 688322841
• Company Name: Meta Biomed Co., Ltd.
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806387805465 [Primary]

FDA Product Code

• EKM: Gutta-Percha

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: 2022-10-03
• Device Publish Date: 2022-09-24

On-Brand Devices [Gutta Percha F1/F2/F3]

• 08806387805700: Gutta Percha Points and Bars, F1/F2/F3, 60Points, P 71
• 08806387805465: Gutta Percha Points and Bars, Aurum Pro F1/F2/F3, 60 Points, P 71