Aladuck405 V100 220-21

GUDID 04560304635729

Aladuck405 V100

SBI PHARMACEUTICALS CO., LTD.

Endoscopic light source unit, line-powered

• Primary Device ID: 04560304635729
• NIH Device Record Key: 22b2b2be-af9f-4770-bc3d-5b3fce3a13e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aladuck405 V100
• Version Model Number: 220-21
• Catalog Number: 220-21
• Company DUNS: 712583343
• Company Name: SBI PHARMACEUTICALS CO., LTD.
• 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	04560304635729 [Primary]

FDA Product Code

• NTN: Led Light Source

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: 2023-05-10
• Device Publish Date: 2023-05-02

Devices Manufactured by SBI PHARMACEUTICALS CO., LTD.

• 04560304635774 - Universal Filter: 2023-05-23
• 04560304635729 - Aladuck405 V100: 2023-05-10Aladuck405 V100
• 04560304635729 - Aladuck405 V100: 2023-05-10 Aladuck405 V100
• 04560304635736 - Aladuck405 V220: 2023-05-10 Aladuck405 V220
• 04560304635743 - AladuckII V100: 2023-05-10 AladuckII V100
• 04560304635750 - AladuckII V220: 2023-05-10 AladuckII V220