Precise Diamond

GUDID M896PRCDIA1201

Precise Diamond - 120 mL LP Kit

ARTERIOCYTE MEDICAL SYSTEMS, INC.

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• Primary Device ID: M896PRCDIA1201
• NIH Device Record Key: b1218e75-2e6b-48a5-a215-d7321c74116e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Precise Diamond
• Version Model Number: PRC-DIA-120
• Company DUNS: 809012870
• Company Name: ARTERIOCYTE MEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M896PRCDIA1200 [Primary]
HIBCC	M896PRCDIA1201 [Package]; Contains: M896PRCDIA1200; Package: [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• BK200540

FDA Product Code

• ORG: Platelet And Plasma Separator For Bone Graft Handling

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-07
• Device Publish Date: 2023-05-30

On-Brand Devices [Precise Diamond ]

• M896PRCDIA1201: Precise Diamond - 120 mL LP Kit
• M896PRCDIA0600: Precise Diamond - 60 mL LP Kit