C-KUP Liquefaction Test Cup

GUDID 44719874740779

BONRAYBIO CO., LTD.

General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium

• 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