| Primary Device ID | 26942284606791 |
| NIH Device Record Key | e37caeb9-f025-44ea-bd95-fb80e7c192d0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MD |
| Version Model Number | DBP-6282B |
| Company DUNS | 544392778 |
| Company Name | JOYTECH HEALTHCARE CO.,LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06942284606797 [Primary] |
| GS1 | 26942284606791 [Package] Contains: 06942284606797 Package: [24 Units] In Commercial Distribution |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-08-14 |
| Device Publish Date | 2025-08-06 |
| 16942284601461 - SEJOY | 2026-04-01 |
| 26942284601482 - SEJOY | 2026-04-01 |
| 26942284601499 - SEJOY | 2026-04-01 |
| 26942284601505 - SEJOY | 2026-04-01 |
| 26942284601512 - SEJOY | 2026-04-01 |
| 26942284601529 - SEJOY | 2026-04-01 |
| 26942284601864 - SEJOY | 2026-04-01 |
| 16942284601874 - SEJOY | 2026-04-01 |