SAINING

GUDID 26975482450163

Zhejiang Saining Biotechnology Co., Ltd

Pipette tip

• Primary Device ID: 26975482450163
• NIH Device Record Key: c8c72eb4-30ad-402c-a43f-9b4ef8ac26dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAINING
• Version Model Number: AS3101004
• Company DUNS: 702834723
• Company Name: Zhejiang Saining Biotechnology Co., Ltd
• Device Count: 576
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975482450169 [Unit of Use]
GS1	26975482450163 [Primary]

FDA Product Code

• MXT: Device, Accessory, Cooling Plate For Tissue Embedding Station

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: 2024-04-30
• Device Publish Date: 2024-04-22