Sunmark - McKesson

GUDID 60038703920518

Heating Pad

MCKESSON CORPORATION

Electric pad localized-body heating system

• Primary Device ID: 60038703920518
• NIH Device Record Key: d99cb733-63ba-429b-a0bb-060d5b749ea0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunmark - McKesson
• Version Model Number: 000731-501-000U
• Company DUNS: 177667227
• Company Name: MCKESSON 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: false
• Serial Number: false
• Manufacturing Date: true
• 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	00038703920516 [Primary]
GS1	60038703920518 [Package]; Contains: 00038703920516; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• IRT: Pad, Heating, Powered

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: 2020-06-11
• Device Publish Date: 2016-12-15

On-Brand Devices [Sunmark - McKesson]

• 60038703920525: Heating Pad
• 60038703920518: Heating Pad