Arjo Lateral Transfer Mat

GUDID 10816317023451

Arjo Maxi Air Matrress XL width 39"

RENU MEDICAL, INC

Patient transfer sliding mat

• Primary Device ID: 10816317023451
• NIH Device Record Key: c9db3896-45dd-4c8c-a871-2b192aa350d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arjo Lateral Transfer Mat
• Version Model Number: RM-MAS015000
• Company DUNS: 100439103
• Company Name: RENU MEDICAL, 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: false
• Device Combination Product: false
• Single Use: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816317023454 [Primary]
GS1	10816317023451 [Package]; Contains: 00816317023454; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• FMR: Device, Transfer, Patient, Manual

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: 2023-07-14
• Device Publish Date: 2023-07-06

On-Brand Devices [Arjo Lateral Transfer Mat]

• 10816317023451: Arjo Maxi Air Matrress XL width 39"
• 10816317023444: Arjo Maxi Air Matrress L width 34"