| Primary Device ID | 00892064002294 |
| NIH Device Record Key | fc05dda8-9487-43b1-8b62-fd547733b3a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kahook Dual Blade |
| Version Model Number | KDB |
| Catalog Number | KDB |
| Company DUNS | 622768711 |
| Company Name | NEW WORLD MEDICAL, INCORPORATED |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00892064002294 [Primary] |
| HNN | Knife, ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
[00892064002294]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-07-13 |
| Device Publish Date | 2016-11-22 |
| 00892064002362 - VIA360 Surgical System | 2025-02-26 VIA360 Surgical System |
| 00892064002102 - Streamline Surgical System | 2025-02-24 Streamline |
| 00892064002089 - Ahmed ClearPath ST | 2024-12-26 Glaucoma shunt |
| 00892064002096 - Ahmed ClearPath ST | 2024-12-26 Glaucoma shunt |
| 00892064002072 - Streamline® Surgical System | 2023-11-09 Streamline |
| 00892064002331 - Ahmed Tube Inserter | 2022-10-05 Tube Inserter |
| 00892064002010 - Streamline® Surgical System | 2021-11-09 Streamline |
| 00892064002126 - Ahmed™ Glaucoma Valve | 2021-08-05 Pediatric Silicone Glaucoma Drainage Device |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KAHOOK DUAL BLADE 86539734 4864575 Live/Registered |
New World Medical, Inc. 2015-02-19 |