Sensorendo
GUDID 06974723794413
Flexible Video Laryngoscope Model S-FVL
Sensorendo Medical Technology (Zhuhai) Co., Ltd.
Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor Video intubation laryngoscope handle/monitor| Primary Device ID | 06974723794413 |
| NIH Device Record Key | 31552173-3a76-4fb0-8269-0cc0baf6b00f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sensorendo |
| Version Model Number | S-FVL |
| Company DUNS | 722337994 |
| Company Name | Sensorendo Medical Technology (Zhuhai) 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com | |
| Phone | +8613602561980 |
| info@sensorendo.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06974723794413 [Primary] |
| GS1 | 16974723794410 [Package] Package: [5 Units] In Commercial Distribution |
FDA Product Code
| CAL | Laryngoscope, Non-Rigid |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
[06974723794413]
Liquid Chemical
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-21 |
| Device Publish Date | 2022-11-11 |
On-Brand Devices [Sensorendo]
| 06974723794413 | Flexible Video Laryngoscope Model S-FVL |
| 06974723792112 | Model S-VL-01 Video Laryngoscope |
| 06974723791115 | Video Stylet Model: S-RVL |
| 06974723796011 | Single Use Flexible Video Laryngoscope Model S-DVL |
| 16974723795950 | Video Laryngoscope Display DP10 |
Trademark Results [Sensorendo]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SENSORENDO 97695176 not registered Live/Pending |
Sensorendo Medical Technology (Zhuhai) Co.,Ltd. 2022-11-29 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.