GUDID 16959664911195

Hangzhou AGS MedTech Co., Ltd.

Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use Flexible endoscopic tissue manipulation forceps, single-use

• Primary Device ID: 16959664911195
• NIH Device Record Key: e5edd0e6-f4bd-4034-bbf9-40ea23fd1ade
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: AG-50310-2323
• Company DUNS: 542984702
• Company Name: Hangzhou AGS MedTech 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: 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	06959664911198 [Primary]
GS1	16959664911195 [Package]; Contains: 06959664911198; Package: box [10 Units]; In Commercial Distribution
GS1	26959664911192 [Package]; Package: carton [100 Units]; In Commercial Distribution

FDA Product Code

• PTS: Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt

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: 2022-10-17
• Device Publish Date: 2022-10-09

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