| Primary Device ID | 10697660001095 |
| NIH Device Record Key | f4811f17-2f82-4462-a1f2-8aa0bdb03a3d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bilateral Conformer 18/20 Small |
| Version Model Number | 19-102 |
| 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 514-381-3292 |
| sales@oculoplastik.com |
| Depth | 4 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10697660001095 [Primary] |
| HIBCC | M8721910207 [Previous] |
| HQN | Conformer, Ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10697660001095]
Hydrogen Peroxide;Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-29 |
| Device Publish Date | 2019-10-21 |
| 10697660001095 | Conformers (made of acrylic or PMMA) are single use devices. They are used to keep the form of t |
| M8721910207 | Conformers (made of acrylic or PMMA) are single use devices. They are used to keep the form of t |