Starplex

GUDID 00840165400754

30 ml Collector, White Cap, Sterile.

Pretium Canada Packaging ULC

General specimen container IVD, no additive/medium

• Primary Device ID: 00840165400754
• NIH Device Record Key: 46132ed1-f187-4a4e-9fe0-9d0cd1bf4fee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Starplex
• Version Model Number: V302
• Company DUNS: 246665038
• Company Name: Pretium Canada Packaging ULC
• Device Count: 200
• 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: false
• Serial Number: false
• Manufacturing Date: false
• 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
GS1	00840165400747 [Primary]
GS1	00840165400754 [Package]; Contains: 00840165400747; Package: [5 Units]; In Commercial Distribution
GS1	10840165400744 [Unit of Use]

FDA Product Code

• FMH: Container, Specimen, Sterile

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: 2025-03-03
• Device Publish Date: 2025-02-21

On-Brand Devices [Starplex ]

• 10840165400874: 10 ml Vial with White Cap, Individually Peel Packed, Sterile.
• 00840165400754: 30 ml Collector, White Cap, Sterile.
• 00840165400976: Specimen Container, 30 ml, Fecal Spork, Non-Sterile.
• 10840165400867: 10 ml Urine Preservative Vial, for Urine Culture and Urinalysis, Sterile