babaka

GUDID 06950715503294

Back Brace

Cofoe Medical Technology Co.,Ltd

Lumbar spine orthosis

• Primary Device ID: 06950715503294
• NIH Device Record Key: b8d044cc-750f-4f9a-b38c-0e7abd52bd03
• Commercial Distribution Discontinuation: 2030-04-27
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: babaka
• Version Model Number: New E+
• Company DUNS: 544425204
• Company Name: Cofoe Medical Technology 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	06950715503294 [Primary]

FDA Product Code

• IPT: Orthosis, Thoracic

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: 2024-07-22
• Device Publish Date: 2024-07-12

On-Brand Devices [babaka]

• 06950715503294: Back Brace
• 06950715503287: Back Brace
• 06950715503270: Lumbar Support
• 06950715504444: Back Brace
• 06950715504437: Back Brace
• 06950715504512: Back Brace
• 06950715504505: Back Brace
• 06950715505564: Back Brace