DRSHD 1080p

GUDID 00817613020147

Accessory Pack for DRSHD Rev. 7

MED X CHANGE, INC.

Electrical mains power extension cable

• Primary Device ID: 00817613020147
• NIH Device Record Key: 40343a4e-3e08-41a1-bb6e-03851a64429c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRSHD 1080p
• Version Model Number: P-DRSHD.7
• Company DUNS: 051244569
• Company Name: MED X CHANGE, INC.
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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	00817613020147 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2018-02-23

On-Brand Devices [DRSHD 1080p]

• 00817613020383: DRSHD 1080p System, Rev 7
• 00817613020147: Accessory Pack for DRSHD Rev. 7
• 00817613020000: DRSHD 1080p System, Rev 7https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml#