YELLOW 560

GUDID 04049539104359

for OPMI PENTERO 800 and OPMI PENTERO 900

Carl Zeiss Meditec AG

Neurosurgical microscope

• Primary Device ID: 04049539104359
• NIH Device Record Key: c4634495-f4cd-4bc9-a7a3-1eafbfb0a104
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: YELLOW 560
• Version Model Number: 302582-9205-000
• Company DUNS: 342228620
• Company Name: Carl Zeiss Meditec AG
• 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: false
• Manufacturing Date: true
• 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	04049539104359 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162991

FDA Product Code

• IZI: System, X-Ray, Angiographic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-21
• Device Publish Date: 2018-02-16

On-Brand Devices [YELLOW 560]

• 04049539104359: for OPMI PENTERO 800 and OPMI PENTERO 900
• 04049539070166: accessory for surgical microscopes