| Primary Device ID | 04560224989230 |
| NIH Device Record Key | 5bdc9df4-08fa-411f-81ba-566378e90279 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NL400 |
| Version Model Number | NL400MCB |
| Company DUNS | 690710546 |
| Company Name | NAKANISHI INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04560224989230 [Primary] |
| EBW | Controller, foot, handpiece and cord |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04560224989230]
Moist Heat or Steam Sterilization
[04560224989230]
Moist Heat or Steam Sterilization
[04560224989230]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-29 |
| Device Publish Date | 2020-06-19 |
| 04560224989254 | NL400CDB |
| 04560224989230 | NL400MCB |
| 04560224989223 | NL400CMC |
| 04560264574038 | NL400SBSET2BEL |
| 04560264573772 | NL400S120E |
| 04560264573260 | TI-MAX NL400 CONTROL BOX |
| 04560264572959 | NL400CDE |
| 04560264572850 | NL400 |
| 04560264572843 | NL400CD |