| Primary Device ID | 33760087120715 |
| NIH Device Record Key | dc5c735c-9186-4cd2-ac85-5b8a8353b61d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Eyelid weight, implantable |
| Version Model Number | PTOSIS SLING SET LLOUQUET & GUERIN, M. D. |
| Catalog Number | S3.1000u |
| Company DUNS | 763408366 |
| Company Name | FCI S A S FCI 20 22 |
| Device Count | 3 |
| 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 | true |
| 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 |
| Phone | 800-932-4202 |
| orders@fci-ophthalmics.com |
| Length | 280 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03760087120714 [Primary] |
| GS1 | 33760087120715 [Unit of Use] |
| HJZ | Crutch, Ptosis |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[33760087120715]
Radiation Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-03-05 |
| Device Publish Date | 2020-02-26 |
| 03760087120806 | An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the e |
| 03760087120721 | An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the e |
| 33760087120715 | An ophthalmic device that is implanted subcutaneously within the upper eyelid to "lidload" the e |