Tianbo

GUDID 06974712700012

NINGBO TIANBO FIRST AID PRODUCT CO.,LTD.

First aid kit, non-medicated, single-use

• Primary Device ID: 06974712700012
• NIH Device Record Key: b6276b36-9fb1-4e16-b967-3af867265862
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tianbo
• Version Model Number: FA12
• Company DUNS: 413680615
• Company Name: NINGBO TIANBO FIRST AID PRODUCT 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: false
• 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	06974712700012 [Primary]

FDA Product Code

• OHO: First Aid Kit Without Drug

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: 2021-12-03
• Device Publish Date: 2021-11-25