Selectis

GUDID B57261059AB0

EMERALD SUPPLIES INC

Low-air-loss bed

• Primary Device ID: B57261059AB0
• NIH Device Record Key: 24c92828-2b6e-4a0d-9ec1-f04e24abad27
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Selectis
• Version Model Number: 61059AB
• Company DUNS: 080689611
• Company Name: EMERALD SUPPLIES 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: false
• Manufacturing Date: false
• 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
HIBCC	B57261059AB0 [Primary]

FDA Product Code

• FNM: Mattress, Air Flotation, Alternating Pressure

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: 2020-03-05
• Device Publish Date: 2020-02-26

On-Brand Devices [Selectis]

• B572610620: 61062
• B572610610: 61061
• B572610590: 61059
• B572610580: 61058
• B572610570: 61057
• B57261759AB0: 61759AB
• B572617580: Alternating Pressure Mattress System
• B572614620: 61462
• B572614610: 61461
• B57261459AB0: 61459AB
• B572614580: Alternating Pressure Mattress System
• B57261059AB0: 61059AB
• B572116000: 11600
• B57261061AB0: Alternating Pressure Low Air Loss System