WEGO

GUDID 26932992110581

Shandong Weigao Group Medical Polymer Co., Ltd.

Metered-delivery hypodermic syringe

• Primary Device ID: 26932992110581
• NIH Device Record Key: 34ad998f-fdeb-40c9-bc38-63f10b0a962e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WEGO
• Version Model Number: 1ml
• Company DUNS: 421533514
• Company Name: Shandong Weigao Group Medical Polymer Co., Ltd.
• 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: false
• 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	06932992110587 [Unit of Use]
GS1	16932992110584 [Primary]
GS1	26932992110581 [Package]; Contains: 16932992110584; Package: Carton [20 Units]; In Commercial Distribution
GS1	36932992110588 [Package]; Package: CARTON [15 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072739

FDA Product Code

• FMF: Syringe, Piston

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: 2020-12-11
• Device Publish Date: 2020-12-03

On-Brand Devices [WEGO]

• 26932992110581: 1ml
• 16932992110591: 3ml
• 26932992110604: 1ml 23Gx1
• 26932992110949: 1ml LL with 23G needle
• 26932992110925: 1ml LL with 25Gx1 needle
• 26932992110871: 1ml LL