everpure

GUDID 06975803581237

SHANGHAI EVERPURE PLASTICS CO., LTD.

General specimen container IVD, no additive/medium

• Primary Device ID: 06975803581237
• NIH Device Record Key: 3a9a4711-2b37-4dc1-8851-32b4bb069027
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: everpure
• Version Model Number: DYND36600
• Company DUNS: 711057027
• Company Name: SHANGHAI EVERPURE PLASTICS CO., LTD.
• 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
GS1	06975803581237 [Primary]

FDA Product Code

• NNI: Container, Specimen, 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: 2022-11-16
• Device Publish Date: 2022-11-08