Primary Device ID | 06972197483437 |
NIH Device Record Key | 89eb7918-be8f-412b-b87e-6a3d7264f95f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Single-use Ureteral Access Sheath |
Version Model Number | UA-S1803 |
Company DUNS | 554484862 |
Company Name | Hunan Vathin Medical Instrument 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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 06972197483437 [Primary] |
FED | Endoscopic Access Overtube, Gastroenterology-Urology |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-08-18 |
Device Publish Date | 2025-08-08 |
06972197482317 | UA-S1D01 |
06972197482300 | UA-S1D00 |
06972197482294 | UA-S1C01 |
06972197482287 | UA-S1C00 |
06972197482270 | UA-S1B01 |
06972197482263 | UA-S1B00 |
06972197482256 | UA-S1A01 |
06972197482249 | UA-S1A00 |
06972197482232 | UA-S1801 |
06972197482225 | UA-S1800 |
06972197483512 | UA-S1D03 |
06972197483505 | UA-S1D02 |
06972197483499 | UA-S1C03 |
06972197483482 | UA-S1C02 |
06972197483475 | UA-S1B03 |
06972197483468 | UA-S1B02 |
06972197483451 | UA-S1A03 |
06972197483444 | UA-S1A02 |
06972197483437 | UA-S1803 |
06972197483420 | UA-S1802 |