Primary Device ID | 16938327906341 |
NIH Device Record Key | 1d77846e-a9ab-4f04-b8cf-bfb0d71ba94a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guerbet |
Version Model Number | 700207-1C |
Catalog Number | 249053 |
Company DUNS | 529174252 |
Company Name | Shenzhen Boon Medical Supply 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 |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com | |
Phone | 9999999999 |
client.complaint@guerbet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06938327906344 [Primary] |
GS1 | 16938327906341 [Package] Contains: 06938327906344 Package: box [50 Units] In Commercial Distribution |
GS1 | 26938327906348 [Package] Package: carton [2 Units] In Commercial Distribution |
DXT | Injector And Syringe, Angiographic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-08 |
Device Publish Date | 2024-10-31 |
26938327906164 | OPTIV SU 1XSYR200ML Y-COIL150CM 2V J X50 Optivantage® CT Syringe with Dual Check Valve Y tubing |
26938327906157 | OPTIV SU/OPO 1XSYR200ML COIL150CM J X50 Optivantage® / OptiOne® CT Syringe with Handi-Fil stra |
26938327906300 | OPTIV SU 2XSYR200ML Y-COIL150CM 2V S X20 Optivantage® Dual CT Syringe with Dual Check Valve Y |
26938327906294 | OPTIV SU 2XSYR200ML Y-COIL150CM OV S X20 Optivantage® Dual CT Syringe with Y tubing (60"/1500m |
26938327906287 | OPTIV SU 1XSYR200ML Y-COIL150CM 2V S X50 Optivantage® CT Syringe with Dual Check Valve Y tubin |
26938327906270 | OPTIV SU/OPO 1XSYR200ML COIL150CM S X50 Optivantage®/ OptiOne® CT Syringe with Coiled Tube(60" |
26938327906195 | OPTIS SU 2XSYR60ML Y-COIL150CM S X50 Optistar Elite®Dual MR syringe with Single Check Valve Y |
26938327906188 | OPTIV SU 2XSYR200ML Y-COIL150CM 2V J X20 Optivantage®Dual CT Syringe with Dual Check Valve Y tu |
26938327906171 | OPTIV SU 2XSYR200ML Y-COIL150CM OV J X20 Optivantage ® Dual CT Syringe with Y tubing (60"/1500m |
16938327906341 | 1-21'' Transfer Set with Swabable Valve and Vented Spike |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUERBET 76380991 2770911 Dead/Cancelled |
Guerbet 2002-03-09 |
GUERBET 73622877 1620762 Dead/Cancelled |
GUERBET S.A. 1986-09-29 |