sentida 7-i

GUDID 04050621100005

Basic electric home bed

WISSNER-BOSSERHOFF GmbH

Basic electric home bed

• Primary Device ID: 04050621100005
• NIH Device Record Key: d0951e40-7c70-4e21-b044-bb7f065b57b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: sentida 7-i
• Version Model Number: 19-1061
• Company DUNS: 340866990
• Company Name: WISSNER-BOSSERHOFF GmbH
• 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	04050621100005 [Primary]

FDA Product Code

• LLI: Bed, Therapeutic, Ac-Powered, Adjustable Home-Use

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: 2019-11-21
• Device Publish Date: 2019-11-13

Devices Manufactured by WISSNER-BOSSERHOFF GmbH

• 04050621100555 - sentida 5 xxl: 2024-09-06
• 04050621100609 - sentida sc-xl USA: 2024-09-06
• 04050621100616 - sentida sc-xxl USA: 2024-09-06
• 04050621100593 - sentida sc USA: 2023-09-21
• 04050621100432 - sentida 04: 2023-01-12 Basic electric home bed
• 04050621100463 - sentida 6-xl: 2023-01-12 Basic electric home bed
• 04050621100470 - sentida 5-le: 2023-01-12
• 04050621100487 - sentida 6-le: 2023-01-12 Basic electric home bed