SEER

GUDID 04987382233942

SUZUKEN CO., LTD.

Electrocardiograph, professional, multichannel

• Primary Device ID: 04987382233942
• NIH Device Record Key: b74bf60e-f277-4b4e-8aac-2b8e19d3ce9d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SEER
• Version Model Number: SEER Light Patient Cable 3CH IEC
• Company DUNS: 690583984
• Company Name: SUZUKEN 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: true
• 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	04987382233942 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021470

FDA Product Code

• MWJ: Electrocardiograph,Ambulatory(Without Analysis)

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: 2020-02-19
• Device Publish Date: 2016-10-06

On-Brand Devices [SEER]

• 04987382233966: SEER Light Patient Cable 3CH IEC-Short
• 04987382233959: SEER Light Patient Cable 2CH IEC-Short
• 04987382233942: SEER Light Patient Cable 3CH IEC
• 04987382233935: SEER Light Patient Cable 2CH IEC CF
• 04987382233928: SEER Light Patient Cable 3CH AHA-Short
• 04987382233911: SEER Light Patient Cable 2CH AHA-Short
• 04987382233904: SEER Light Patient Cable 3CH AHA
• 04987382233898: SEER Light Patient Cable 2CH AHA CF
• 00840682108249: Light Connect
• 00840682108225: Light Extend
• 00840682108195: Light Extend Controller
• 00840682108188: Light