E-Z Draw Sample Port

GUDID 10858293006400

REPROCESSING PRODUCTS CORPORATION

Haemodialysis treatment kit

• Primary Device ID: 10858293006400
• NIH Device Record Key: 748c0218-cd66-4879-b7a8-dfeeb584b754
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-Z Draw Sample Port
• Version Model Number: D300-2010
• Company DUNS: 796083392
• Company Name: REPROCESSING PRODUCTS CORPORATION
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• 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	00858293006403 [Primary]
GS1	10858293006400 [Package]; Contains: 00858293006403; Package: Bag [100 Units]; In Commercial Distribution

FDA Product Code

• MON: System, Hemodialysis, Remote Accessories

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: 2019-08-30
• Device Publish Date: 2019-08-22

On-Brand Devices [E-Z Draw Sample Port]

• 10858293006400: D300-2010
• 00858293006847: D300-2011 E-Z Draw Sample Port