Polaris 600

GUDID 04048675416562

Drägerwerk AG & Co. KGaA

Operating light

• Primary Device ID: 04048675416562
• NIH Device Record Key: 6a0a65cb-fc42-4b17-bcb1-52fca8470f65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Polaris 600
• Version Model Number: G16720
• Company DUNS: 315578914
• Company Name: Drägerwerk AG & Co. KGaA
• 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: 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

Customer Support Contacts

• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM
• Phone: +494518820
• Email: INFO@DRAEGER.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	04048675416562 [Primary]

FDA Product Code

• FTD: Lamp, Surgical

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: 2016-06-03

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• 04048675564577 - T-piece N for Nebulization: 2024-10-16