Primary Device ID | 13700773727268 |
NIH Device Record Key | 5453eb56-f1b2-48f1-9962-419f7cda8f1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OCULID GOLD 1,8g |
Version Model Number | S3.3018 |
Company DUNS | 763408366 |
Company Name | FCI S A S FCI 20 22 |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 13700773727268 [Primary] |
NCB | Weights, Eyelid, Implantable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-16 |
Device Publish Date | 2022-03-08 |
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