GUDID 16959664911850

Hangzhou AGS MedTech Co., Ltd.

Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 16959664911850
• NIH Device Record Key: d33be23f-f6bb-48d7-82ee-881a008471c1
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AG-5078-241523
• Company DUNS: 542984702
• Company Name: Hangzhou AGS MedTech 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06959664911853 [Primary]
GS1	16959664911850 [Package]; Contains: 06959664911853; Package: box [10 Units]; In Commercial Distribution
GS1	26959664911857 [Package]; Package: carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K172729

FDA Product Code

• FDI: Snare, Flexible

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: 2022-10-18
• Device Publish Date: 2022-10-10

Devices Manufactured by Hangzhou AGS MedTech Co., Ltd.

• 16959664911959 - NA: 2023-04-10
• 16959664911966 - NA: 2023-04-10
• 16959664913496 - NA: 2023-04-10
• 16959664934279 - NA: 2023-04-10
• 16959664934316 - NA: 2023-04-10
• 16959664902087 - NA: 2022-10-20
• 16959664902100 - NA: 2022-10-20
• 16959664902162 - NA: 2022-10-20