E-Z Draw Sample Port

GUDID 10858293006400

REPROCESSING PRODUCTS CORPORATION

Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit Haemodialysis treatment kit 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