Gutta Percha D-XF

GUDID 08806387806417

Gutta percha points and bars D-XF, 100 Points, P 51

Meta Biomed Co., Ltd.

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• Primary Device ID: 08806387806417
• NIH Device Record Key: ce938dcc-2227-4dca-8bba-556a7baa3439
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gutta Percha D-XF
• Version Model Number: 0641
• 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	08806387806417 [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 D-XF]

• 08806387806639: Gutta Percha Points and Bars D-XF, 120 Points, P 51
• 08806387806417: Gutta percha points and bars D-XF, 100 Points, P 51