Battery Module

GUDID 07325710003138

Maquet Critical Care AB

Neonatal/adult intensive-care ventilator

• Primary Device ID: 07325710003138
• NIH Device Record Key: de7a2555-ce60-44d9-a27b-ae566b7cf0fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Battery Module
• Version Model Number: 6487180
• Company DUNS: 632707092
• Company Name: Maquet Critical Care AB
• Device Count: 1
• DM Exempt: false
• 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: 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	07325710003138 [Primary]

FDA Product Code

• CBK: Ventilator, Continuous, Facility Use

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: 2015-10-22

On-Brand Devices [Battery Module]

• 07325710003138: 6487180
• 07325710003909: 6882607