Anesthesia frame

GUDID 07350111830922

Reison Medical AB

Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen Anaesthesia screen

• Primary Device ID: 07350111830922
• NIH Device Record Key: 2377002b-6394-48d4-9b5b-d55624bc828b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anesthesia frame
• Version Model Number: 10-311-16
• Company DUNS: 356766220
• Company Name: Reison Medical AB
• 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: true
• Serial Number: false
• 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	07350111830922 [Primary]

FDA Product Code

• FWZ: Operating Room Accessories Table Tray

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: 2022-05-09
• Device Publish Date: 2022-04-30

On-Brand Devices [Anesthesia frame]

• 07350111830946: 10-311-US
• 07350111830939: 10-311-UK
• 07350111830922: 10-311-16
• 07350111830915: 10-311
• 07350111830908: 10-310