MINICAP WITH POVIDONE-IODINE SOLUTION 5C4466P

GUDID 50085412007699

This device is a plastic disconnect cap for peritoneal dialysis and contains povidone-iodine intended to protect the female Luer connector of the Baxter transfer set.

BAXTER HEALTHCARE CORPORATION

Peritoneal dialysis system tubing set

• Primary Device ID: 50085412007699
• NIH Device Record Key: d6c3779b-8d07-48c9-ac63-4369f68ce95b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MINICAP WITH POVIDONE-IODINE SOLUTION
• Version Model Number: 5C4466P
• Catalog Number: 5C4466P
• Company DUNS: 005083209
• Company Name: BAXTER HEALTHCARE CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)933-0303
• Email: Medinfo_medproducts@baxter.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store at room temperature no more than 30Deg Celcius. Avoid excessive heat.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00085412007694 [Primary]
GS1	50085412007699 [Package]; Contains: 00085412007694; Package: CASE [60 Units]; In Commercial Distribution

FDA Product Code

• KDJ: SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-12
• Device Publish Date: 2015-10-07

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