| Primary Device ID | 00813059018328 |
| NIH Device Record Key | 423fb664-f0c5-49db-b7c6-4e753021666e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Diamatrix Ltd. |
| Version Model Number | H573-D |
| Catalog Number | H573-D |
| Company DUNS | 809555139 |
| Company Name | Diamatrix |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com | |
| Phone | +1 (281) 367-8081 |
| cs@diamatrix.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813059018328 [Primary] |
| HNQ | Hook, Ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
[00813059018328]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-06-23 |
| Device Publish Date | 2022-06-15 |
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