Asensus X9007763
GUDID 17466532979243
Senhance USB-C LIA Drape (X9007763)
DAS Medical International SRL
Medical equipment drape, single-use| Primary Device ID | 17466532979243 |
| NIH Device Record Key | 0db58d80-1e3a-404d-a397-c1ff244fa6ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Asensus |
| Version Model Number | X9007763 |
| Catalog Number | X9007763 |
| Company DUNS | 817435655 |
| Company Name | DAS Medical International SRL |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx | |
| Phone | 809-556-8900 |
| xx@xx.xx |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07466532979246 [Primary] |
| GS1 | 17466532979243 [Package] Contains: 07466532979246 Package: Inner box [10 Units] In Commercial Distribution |
| GS1 | 27466532979240 [Package] Package: Case [3 Units] In Commercial Distribution |
FDA Product Code
| PUI | Drape, Surgical, Exempt |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
[17466532979243]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-18 |
| Device Publish Date | 2021-05-10 |
On-Brand Devices [Asensus]
| 17466532979243 | Senhance USB-C LIA Drape (X9007763) |
| 17466532979236 | Senhance Articulating Drape (X9007762) |
| 17466532979267 | X9007769 Senhance Manipulator Arm Drape w/verification Card, 3 Pack |
| 17466532979250 | X9007768 Senhance Arm Drape, W/ Verification Card |
Trademark Results [Asensus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ASENSUS 90356163 not registered Live/Pending |
Transenterix Surgical, Inc. 2020-12-03 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.