Power adapter

GUDID 06975339626792

MacroLux Medical Technology Co., Ltd.

Endoscopic video image processing unit

• Primary Device ID: 06975339626792
• NIH Device Record Key: e78fdbc2-7199-4848-a859-d12a335e1b23
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Power adapter
• Version Model Number: Type K
• Company DUNS: 723490133
• Company Name: MacroLux Medical Technology Co., Ltd.
• 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: 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	06975339626792 [Primary]

FDA Product Code

• EOQ: Bronchoscope (Flexible Or Rigid)

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: 2025-09-01
• Device Publish Date: 2025-08-23

On-Brand Devices [Power adapter]

• 06975339626808: Type H
• 06975339626792: Type K
• 06975339626778: Type N
• 06975339626761: Type I
• 06975339626754: Type B (Japan)
• 06975339626747: Type L
• 06975339626723: Type B (USA)
• 06975339626716: Type G