CATHETER REPAIR KIT RMS52001

GUDID 30884908158206

CATHETER REPAIR KIT

Medical Components, Inc.

Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated Arterial/central venous catheterization support/maintenance kit, non-medicated

• Primary Device ID: 30884908158206
• NIH Device Record Key: 37281ec6-d8d5-4103-8c5a-335dadd79175
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CATHETER REPAIR KIT
• Version Model Number: RMS52001
• Catalog Number: RMS52001
• Company DUNS: 038000253
• Company Name: Medical Components, Inc.
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com
• Phone: +1(215)256-4201
• Email: clinical@medcompnet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884908158205 [Primary]
GS1	30884908158206 [Package]; Contains: 00884908158205; Package: inner box [5 Units]; In Commercial Distribution
GS1	50884908158200 [Package]; Package: box [4 Units]; In Commercial Distribution

FDA Product Code

• NFK: Kit, repair, catheter, hemodialysis

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-04
• Device Publish Date: 2020-11-26

On-Brand Devices [CATHETER REPAIR KIT]

• 00884908039658: CATHETER REPAIR KIT
• 00884908001891: CATHETER REPAIR KIT
• 30884908158206: CATHETER REPAIR KIT