UMS Universal Tube/Cap

GUDID 00892159002130

Universal Cap

TYPENEX MEDICAL LLC

Centrifuge tube IVD

• Primary Device ID: 00892159002130
• NIH Device Record Key: 7f879a6d-9edc-4916-8721-5ddf20df7535
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UMS Universal Tube/Cap
• Version Model Number: US0201QD
• Company DUNS: 600850213
• Company Name: TYPENEX MEDICAL LLC
• Device Count: 500
• 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	00892159002130 [Unit of Use]
GS1	00892159002147 [Primary]

FDA Product Code

• NNK: Container, Specimen Mailer And Storage, 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: 2022-11-30
• Device Publish Date: 2022-11-22

On-Brand Devices [UMS Universal Tube/Cap]

• 00892159002130: Universal Cap
• 00892159002116: Universal Tube