Primary Device ID | 00814899027075 |
NIH Device Record Key | 7496abec-3337-4c6f-91a5-2a12806837bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | bioli™ IOL Delivery System |
Version Model Number | BIOLI-D |
Company DUNS | 611655440 |
Company Name | AST PRODUCTS, INC. |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814899027075 [Unit of Use] |
GS1 | 10814899027072 [Primary] |
MSS | Folders And Injectors, Intraocular Lens (Iol) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-15 |
Device Publish Date | 2020-12-07 |
00814899027136 | The bioli™ IOL Delivery System is a single-use, sterile device intended to insert an approved |
00814899027129 | The bioli™ IOL Delivery System is a single-use, sterile device intended to insert an approved |
00814899027075 | The bioli™ IOL Delivery System is a single-use, sterile device intended to insert an approved |
00814899027167 | The bioli™ IOL Delivery System is a single-use, sterile device intended to insert an approved |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOLI 79343259 not registered Live/Pending |
Nina Wiberg Møller 2022-05-31 |