HoverSling Repositioning Sheet

GUDID 10816317023802

HoverSling Repositioning Sheet HMSLING-50RS-B

RENU MEDICAL, INC

General-purpose patient lifting system sling/harness

• Primary Device ID: 10816317023802
• NIH Device Record Key: ccd84a87-f937-48ae-81fe-869e3fee2ced
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HoverSling Repositioning Sheet
• Version Model Number: RM-HMSLING-50RS-B
• 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816317023805 [Primary]
GS1	10816317023802 [Package]; Contains: 00816317023805; Package: case [5 Units]; In Commercial Distribution

FDA Product Code

• FSA: Lift, Patient, Non-Ac-Powered

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: 2020-04-27
• Device Publish Date: 2020-04-17

On-Brand Devices [HoverSling Repositioning Sheet]

• 10816317023802: HoverSling Repositioning Sheet HMSLING-50RS-B
• 00816317023799: HoverSling Repositioning Sheet HMSLING-39RS-B