EndoClot PHS

GUDID 26972011720025

EndoClot Plus Co.,Ltd.

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• Primary Device ID: 26972011720025
• NIH Device Record Key: b470e2e6-b631-4eee-b4ca-dcd38353fbfe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EndoClot PHS
• Version Model Number: EPK2303
• Company DUNS: 544357082
• Company Name: EndoClot Plus 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	16972011720028 [Primary]
GS1	26972011720025 [Package]; Contains: 16972011720028; Package: [1 Units]; In Commercial Distribution

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-01
• Device Publish Date: 2021-06-23

On-Brand Devices [EndoClot PHS]

• 26972011720032: EPK2305
• 26972011720025: EPK2303