| Primary Device ID | 13700773727589 |
| NIH Device Record Key | b3aed787-74d7-49ef-8a8a-e8c7741adf51 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ADHESIVE STRIPS |
| Version Model Number | S3.0500 |
| Company DUNS | 763408366 |
| Company Name | FCI S A S FCI 20 22 |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 13700773727589 [Primary] |
| MML | Weights, Eyelid, External |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-16 |
| Device Publish Date | 2022-03-08 |
| 13700773724397 - EZYPOR® Ø 18 mm | 2024-07-01 Orbital implant |
| 13700773724403 - EZYPOR® Ø 20 mm | 2024-07-01 Orbital implant |
| 13700773724410 - EZYPOR® Ø 22 mm | 2024-07-01 Orbital implant |
| 13700773728081 - EZYPOR® Ø 16 mm | 2024-07-01 Orbital implant |
| 13700773728852 - EZYPOR® Ø 12 mm | 2024-07-01 Orbital implant |
| 13700773728890 - EZYPOR® Ø 14 mm | 2024-07-01 Orbital implant |
| 13700773735096 - OPHTACATH® 2 mm Unilateral Kit | 2024-01-05 A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic |
| 13700773735102 - OPHTACATH® 2 mm Bilateral Kit | 2024-01-05 A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic |