Baru

GUDID 06975783730038

Baru Foshan medical technology co., Limited

Synthetic gutta-percha

• Primary Device ID: 06975783730038
• NIH Device Record Key: c9991393-65f6-4c4b-98b1-533e8735f400
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Baru
• Version Model Number: 6
• Company DUNS: 703931814
• Company Name: Baru Foshan medical technology co., Limited
• Device Count: 60
• 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	06975783730038 [Unit of Use]
GS1	16975783730035 [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: 2024-04-11
• Device Publish Date: 2024-04-03

On-Brand Devices [Baru]

• 06975783730038: 6
• 06975783730021: 5
• 16975783730011: 4