| Primary Device ID | 16927709404278 |
| NIH Device Record Key | c5399764-ee03-4ddb-b50f-44e733fdc2da |
| Commercial Distribution Discontinuation | 2031-03-18 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mevita |
| Version Model Number | BE21 |
| Company DUNS | 421350239 |
| Company Name | Shenzhen Jamr Medical Technology Co., Ltd. |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06927709404271 [Primary] |
| GS1 | 16927709404278 [Package] Contains: 06927709404271 Package: [20 Units] Discontinued: 2031-03-18 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 | 2026-03-27 |
| Device Publish Date | 2026-03-19 |
| 16927709404278 - Mevita | 2026-03-27 |
| 16927709404278 - Mevita | 2026-03-27 |
| 06927709404127 - Oklar | 2026-02-16 |
| 06927709404202 - HoMedics | 2026-02-16 Upper Arm Blood Pressure Monitor |
| 16927709404100 - Oklar | 2026-01-08 |
| 16927709400034 - Oklar | 2025-12-30 |
| 16978034830133 - tenovi | 2025-12-22 |
| 16978034830140 - tenovi | 2025-12-22 |
| 16927709404087 - Ease Healthcare | 2025-12-05 |