E-Z Draw Sample Port

GUDID 00858293006847

D300-2011 E-Z Draw Sample Port

REPROCESSING PRODUCTS CORPORATION

Haemodialysis treatment kit

• Primary Device ID: 00858293006847
• NIH Device Record Key: f18e5b78-5150-4170-b8d6-b0f235554893
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-Z Draw Sample Port
• Version Model Number: D300-2011
• 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	00858293006847 [Primary]
GS1	00858293006854 [Package]; 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: 2021-04-14
• Device Publish Date: 2021-04-06

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

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