| Primary Device ID | 00892064002003 |
| NIH Device Record Key | f64dfa9f-47d7-4bf1-8d76-49b6943624ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kahook Dual Blade - Glide |
| Version Model Number | KDB Glide |
| Catalog Number | KDB Glide |
| Company DUNS | 622768711 |
| Company Name | NEW WORLD MEDICAL, INCORPORATED |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| 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 |
| Phone | +1(909)466-4304 |
| info@newworldmedical.com | |
| Phone | +1(909)466-4304 |
| info@newworldmedical.com | |
| Phone | +1(909)466-4304 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00892064002003 [Primary] |
| HNN | Knife, ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
[00892064002003]
Radiation Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-21 |
| Device Publish Date | 2020-10-13 |
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