MEDUtrigger

GUDID 04054685091408

WEINMANN Emergency Medical Technology GmbH + Co. KG

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• Primary Device ID: 04054685091408
• NIH Device Record Key: 9fd45591-2d1e-4019-b410-1945f121f90b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDUtrigger
• Version Model Number: 20920
• Company DUNS: 342832477
• Company Name: WEINMANN Emergency Medical Technology GmbH + Co. KG
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04054685091408 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193191

FDA Product Code

• BTL: Ventilator, Emergency, Powered (Resuscitator)

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: 2020-12-15
• Device Publish Date: 2020-12-07

On-Brand Devices [MEDUtrigger]

• 04054685091408: 20920
• 04054685091286: 20900