Easydrip Plus Pen Needles

GUDID 36972857294732

Sandstone Medical (Suzhou) Inc.

Autoinjector needle

• Primary Device ID: 36972857294732
• NIH Device Record Key: 4739459c-4f11-4dce-9faa-d0a768ec028b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Easydrip Plus Pen Needles
• Version Model Number: 02-3108
• Company DUNS: 554500882
• Company Name: Sandstone Medical (Suzhou) Inc.
• Device Count: 100
• 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: 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	06972857294731 [Unit of Use]
GS1	16972857294738 [Primary]
GS1	36972857294732 [Package]; Contains: 16972857294738; Package: [2000 Units]; In Commercial Distribution

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

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: 2025-05-26
• Device Publish Date: 2025-05-17

On-Brand Devices [Easydrip Plus Pen Needles]

• 36972857294749: 02-3206
• 36972857294732: 02-3108