Gutta Percha 08-15/40

GUDID 08806387805335

Gutta Percha Points and Bars 08 taper 15/40, 60 Points, P 71

Meta Biomed Co., Ltd.

Synthetic gutta-percha

• Primary Device ID: 08806387805335
• NIH Device Record Key: bfbb3d4d-c138-48ec-aed7-e95442369965
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gutta Percha 08-15/40
• Version Model Number: 0533
• 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	08806387805335 [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

Devices Manufactured by Meta Biomed Co., Ltd.

• 08806387814603 - MX 02-15: 2025-09-03 MGP, 02 Taper 15, 60 Points, P.71
• 08806387814610 - MX 02-20: 2025-09-03 MGP, 02 Taper 20, 60 Points, P.71
• 08806387814627 - MX 02-25: 2025-09-03 MGP, 02 Taper 25, 60 Points, P.71
• 08806387814634 - MX 02-30: 2025-09-03 MGP, 02 Taper 30, 60 Points, P.71
• 08806387814641 - MX 02-35: 2025-09-03 MGP, 02 Taper 35, 60 Points, P.71
• 08806387814658 - MX 02-40: 2025-09-03 MGP, 02 Taper 40, 60 Points, P.71
• 08806387814665 - MX 04-15: 2025-09-03 MGP, 04 Taper 15, 60 Points, P.71
• 08806387814672 - MX 04-20: 2025-09-03 MGP, 04 Taper 20, 60 Points, P.71