Primary Device ID | 16959664900762 |
NIH Device Record Key | 9e5c8918-6d5c-46d3-92f8-f8d7dcec8255 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NA |
Version Model Number | AG-5062-N2024G |
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 Issuing Agency | Device ID |
---|---|
GS1 | 06959664900765 [Primary] |
GS1 | 16959664900762 [Package] Contains: 06959664900765 Package: box [10 Units] In Commercial Distribution |
GS1 | 26959664900769 [Package] Package: carton [100 Units] In Commercial Distribution |
LQR | Dislodger, Stone, Biliary |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-17 |
Device Publish Date | 2022-10-09 |
16959664912123 | AG-5099-05 |
16959664912055 | AG-5098-0525 |
16959664900830 | AG-5063-S2524G |
16959664900786 | AG-5062-N3024G |
16959664900779 | AG-5062-N2524G |
16959664900762 | AG-5062-N2024G |
16959664900106 | AG-5041-2526 |
16959664900021 | AG-5041-3526 |
16959664900014 | AG-5041-2526 |