| Primary Device ID | 10697660002382 |
| NIH Device Record Key | cf8e0a02-fbaf-406b-9c84-6c9c44dc9765 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symblepharon Ring Conformer Large |
| Version Model Number | 21-416 |
| Company DUNS | 257382580 |
| Company Name | Oculo-Plastik Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 514-381-3292 |
| sales@oculoplastik.com |
| Outer Diameter | 24 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10697660002382 [Primary] |
| HIBCC | M8722141608 [Previous] |
| HQN | Conformer, Ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10697660002382]
Ethylene Oxide;Hydrogen Peroxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-31 |
| Device Publish Date | 2019-10-23 |
| 10697660002382 | The Symblepharon rings are used to prevent retraction of the conjunctiva cul-de-sac. The ring is |
| M8722141608 | The Symblepharon rings are used to prevent retraction of the conjunctiva cul-de-sac. The ring is |