5C4527

GUDID 50085412025365

The Short Nose Clamp for Outlet Port of Plastic Container is designed to facilitate peritoneal dialysis set connector insertion into and removal from, Peritoneal Dialysis Solution in plastic container.

BAXTER HEALTHCARE CORPORATION

Medical tubing clip/clamp, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable Medical tubing clip/clamp, temporary, non-calibrated, reusable

• Primary Device ID: 50085412025365
• NIH Device Record Key: 69540e44-a99f-4488-9a49-15f26a1f0f57
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5C4527
• Catalog Number: 5C4527
• Company DUNS: 005083209
• Company Name: BAXTER HEALTHCARE CORPORATION
• 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: false
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM
• Phone: +1(800)933-0303
• Email: MEDINFO_MEDPRODUCTS@BAXTER.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00085412025360 [Primary]
GS1	50085412025365 [Package]; Contains: 00085412025360; Package: CASE [12 Units]; In Commercial Distribution

FDA Product Code

• FKK: CLAMP, LINE

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: 2019-03-25
• Device Publish Date: 2019-03-15

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