CPT2000 Automated Manifold Kit

GUDID 30841716100339

Model CPT2000 p/n 701324-002 Kit Contents: manifold with saline and contrast ports, saline tubing with spike and hand syringe

ACIST MEDICAL SYSTEMS, INC.

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• Primary Device ID: 30841716100339
• NIH Device Record Key: b2010161-bbc4-4398-ac3c-f505a0fb8b4e
• Commercial Distribution Discontinuation: 2018-05-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CPT2000 Automated Manifold Kit
• Version Model Number: 014623
• Company DUNS: 926684994
• Company Name: ACIST 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841716100335 [Primary]
GS1	30841716100339 [Package]; Contains: 10841716100335; Package: Shelf box [10 Units]; Discontinued: 2018-05-29; Not in Commercial Distribution

FDA Product Code

• DXT: Injector And Syringe, Angiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-15
• Device Publish Date: 2016-09-09

On-Brand Devices [CPT2000 Automated Manifold Kit]

• 30841716100339: Model CPT2000 p/n 701324-002 Kit Contents: manifold with saline and contrast ports, saline tubin
• 30841716100346: Model CPT2000 p/n 701324-004 Kit Contents: manifold with saline and contrast ports, saline tubin