Primary Device ID | 10818255010647 |
NIH Device Record Key | 03780dbb-9203-4dc6-8351-278528be20d4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | N/A |
Catalog Number | 5162 |
Company DUNS | 013486803 |
Company Name | MICROVISION, 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 | false |
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 |
Outer Diameter | 0.64 Millimeter |
Special Storage Condition, Specify | Between 0 and 0 *keep away from direct sunlight |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10818255010647 [Primary] |
GS1 | 30818255010641 [Package] Package: carton [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 | 6 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2018-04-04 |
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