ECLIPSE Ti2-I US

GUDID 04549921600341

NIKON CORPORATION

Inverted-stage light microscope

• Primary Device ID: 04549921600341
• NIH Device Record Key: af93017b-6b0c-49af-a710-6a944bbb4c87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ECLIPSE Ti2-I US
• Version Model Number: MEA54315
• Company DUNS: 695221077
• Company Name: NIKON CORPORATION
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04549921600341 [Primary]

FDA Product Code

• MTX: Microscope And Microscope Accessories, Reproduction, Assisted

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: 2025-07-09
• Device Publish Date: 2025-07-01

Devices Manufactured by NIKON CORPORATION

• 04549921600341 - ECLIPSE Ti2-I US: 2025-07-09
• 04549921600341 - ECLIPSE Ti2-I US: 2025-07-09
• 04549921600020 - ECLIPSE Ti2-U IVF US: 2021-08-31