Primary Device ID | 13700773727350 |
NIH Device Record Key | c5d9e533-4bfc-4a6c-baa3-7d80cf360c87 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OCULID PLATINUM SLIM® 1,0 g |
Version Model Number | S3.6010 |
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 | 13700773727350 [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 |
13700773727350 | OCULID PLATINUM SLIM® 1,0 g |
13700773724663 | OCULID PLATINUM SLIM® 1,0 g |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OCULID PLATINUM SLIM 79327900 not registered Live/Pending |
FRANCE CHIRURGIE INSTRUMENTATION SAS 2021-10-18 |