Manual Bed FL23SM

GUDID 26704820000032

Manual Med/Surg articulated bed.

Umano Medical Inc

Manual hospital bed

• Primary Device ID: 26704820000032
• NIH Device Record Key: b9ed9525-6ecc-4c22-9052-7e5ba26e365d
• Commercial Distribution Discontinuation: 2016-09-21
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Manual Bed
• Version Model Number: FL23SM
• Catalog Number: FL23SM
• Company DUNS: 249675476
• Company Name: Umano 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: 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	16704820000035 [Primary]
GS1	26704820000032 [Package]; Contains: 16704820000035; Package: [1 Units]; Discontinued: 2016-09-21; Not in Commercial Distribution
GS1	36704820000039 [Package]; Contains: 16704820000035; Package: [2 Units]; Discontinued: 2016-09-21; Not in Commercial Distribution

FDA Product Code

• FNJ: Bed, Manual

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: 2016-11-30

On-Brand Devices [Manual Bed]

• 20670482000030: Manual Med/Surg articulated bed.
• 26704820000032: Manual Med/Surg articulated bed.