C-KUP Liquefaction Test Cup

GUDID 44719874740779

BONRAYBIO CO., LTD.

General specimen container IVD, no additive

• Primary Device ID: 44719874740779
• NIH Device Record Key: e7021730-d32d-4f19-9726-4768045ac698
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: C-KUP Liquefaction Test Cup
• Version Model Number: CK0_200pcs-BR USA CORP.
• Company DUNS: 658872369
• Company Name: BONRAYBIO 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: false
• 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	44719874740779 [Primary]

FDA Product Code

• NNI: Container, Specimen, Non-Sterile

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: 2021-07-19
• Device Publish Date: 2021-07-09

On-Brand Devices [C-KUP Liquefaction Test Cup]

• 14719874740723: CK0
• 44719874740779: CK0_200pcs-BR USA CORP.
• 44719874740724: CK0_200pcs