Aespire

GUDID 00840682102261

DATEX-OHMEDA INC

Anaesthesia workstation, general-purpose

• Primary Device ID: 00840682102261
• NIH Device Record Key: 07c049e5-e2d6-472b-80e9-d5d2056c59e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aespire
• Version Model Number: 7900
• Company DUNS: 129501685
• Company Name: DATEX-OHMEDA INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840682102261 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050626

FDA Product Code

• BSZ: Gas-machine, anesthesia

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-23

On-Brand Devices [Aespire]

• 00840682102285: View
• 00840682102261: 7900