Sterex

GUDID 06977918410037

JIANGMEN ELITE MEDICAL EQUIPMENT LTD

Mobile patient lifting system, electrically-powered

• Primary Device ID: 06977918410037
• NIH Device Record Key: 39c09aea-7f28-4abf-861e-0fc43b9a22f2
• Commercial Distribution Discontinuation: 2024-11-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Sterex
• Version Model Number: STR500LB
• Company DUNS: 456839550
• Company Name: JIANGMEN ELITE MEDICAL EQUIPMENT LTD
• 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: true
• 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	06977918410037 [Primary]

FDA Product Code

• FNG: Lift, Patient, 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: 2024-11-26
• Device Publish Date: 2024-11-18

On-Brand Devices [Sterex]

• 06977918410082: STS600
• 06977918410075: STS500
• 06977918410068: STR600LB
• 06977918410051: STR600PB
• 06977918410044: STR500PB
• 06977918410037: STR500LB
• 06977918410020: HOFF750
• 06977918410013: HOFF500