Primary Device ID | B384VS0200275 |
NIH Device Record Key | f3ded9ee-ae3d-412c-bc6f-85055ddccbf1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 27ga Soft Tip Cannula |
Version Model Number | VS0200.27 |
Catalog Number | VS0200.27 |
Company DUNS | 080375891 |
Company Name | Vortex Surgical, Inc. |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B384VS02002719 [Primary] |
HIBCC | B384VS0200275 [Package] Contains: B384VS02002719 Package: [5 Units] In Commercial Distribution |
HMX | Cannula, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-11-21 |
Device Publish Date | 2019-08-27 |
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00810123480074 - Vortex Surgical Inc | 2023-02-13 25ga Illuminated Curved Laser Probe Alcon Box of 5 |
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00810123480098 - Vortex Surgical Inc | 2023-02-13 25ga Illuminated Curved Laser Probe Bausch and Lomb Box of 5 |
00810123480456 - Vortex Surgical Inc | 2023-02-10 Internal Delivery Device (I.D.D.) Box of 5 |
00810123480463 - Vortex Surgical Inc | 2023-02-10 23ga Backflush Box of 5 |