Baha Mar

GUDID 06974675410713

Hunter Amenities (Shantou) Co., Ltd.

Basic manual toothbrush

• Primary Device ID: 06974675410713
• NIH Device Record Key: 287f2d0f-d341-49cc-bfd8-e4cf5627562c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Baha Mar
• Version Model Number: 50916000018
• Company DUNS: 554538623
• Company Name: Hunter Amenities (Shantou) 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	06974675410713 [Primary]

FDA Product Code

• EFW: Toothbrush, Manual

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: 2022-02-25
• Device Publish Date: 2022-02-17

Devices Manufactured by Hunter Amenities (Shantou) Co., Ltd.

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• 06974675410690 - Hyatt(CPE): 2022-02-25
• 06974675410706 - Fairmont Le Labo: 2022-02-25
• 06974675410713 - Baha Mar: 2022-02-25
• 06974675410713 - Baha Mar: 2022-02-25
• 06974675410720 - Edition Hotel: 2022-02-25