Test Tubes, Micro 101521

GUDID G0561015211

Bio/Data Corporation

Assay container IVD, single-use

• Primary Device ID: G0561015211
• NIH Device Record Key: a932206b-dbea-4ea2-873a-b2b207d5e96c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Test Tubes, Micro
• Version Model Number: 101521
• Catalog Number: 101521
• Company DUNS: 051392959
• Company Name: Bio/Data Corporation
• 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: 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
HIBCC	G0561015211 [Primary]

FDA Product Code

• GLE: Mixer, Blood Tube

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: 2023-09-07
• Device Publish Date: 2023-08-30

Devices Manufactured by Bio/Data Corporation

• G0561076501 - AGG/PAK 5 Combo Kit: 2024-10-09
• G0561003361 - Test Tubes, Macro: 2023-09-07
• G0561009890 - Calcium Chloride: 2023-09-07
• G0561009910 - Tris Buffered Saline: 2023-09-07
• G0561009940 - Sodium Citrate: 2023-09-07
• G0561013751 - Profiler Paper: 2023-09-07
• G0561015211 - Test Tubes, Micro: 2023-09-07
• G0561015211 - Test Tubes, Micro: 2023-09-07
• G0561055981 - Printer Paper: 2023-09-07