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 |
Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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Phone | 809-556-8900 |
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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 |
PUI | Drape, Surgical, Exempt |
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
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-18 |
Device Publish Date | 2021-05-10 |
17466532979243 | Senhance USB-C LIA Drape (X9007763) |
17466532979236 | Senhance Articulating Drape (X9007762) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ASENSUS 90356163 not registered Live/Pending |
Transenterix Surgical, Inc. 2020-12-03 |