| Primary Device ID | 04589551354740 |
| NIH Device Record Key | 249519c1-0988-42a1-90d2-e250f2f81377 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PD-CTAD-SM |
| Version Model Number | PD-CTAD-SM |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04589551354740 [Direct Marking] |
| GS1 | 04589551354788 [Primary] |
| HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-18 |
| Device Publish Date | 2022-05-10 |
| 04589551393367 - PANA SPRAY Plus | 2025-10-02 |
| 04560264576940 - SG20M | 2025-09-05 |
| 04560264576957 - X-SG20ML | 2025-09-05 |
| 04589551381500 - NLZ | 2025-09-03 |
| 04589551381517 - NLZ | 2025-09-03 |
| 04589551381531 - NLZ | 2025-09-03 |
| 04589551381562 - NLZ | 2025-09-03 |
| 04589551381586 - NLZ | 2025-09-03 |