| Primary Device ID | 06974246462608 |
| NIH Device Record Key | c4ca3308-249f-4354-9e35-10a31b7170db |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Safecare Vaginal PH Rapid Test Cassette |
| Version Model Number | 5 Tests |
| Catalog Number | PH-6012 |
| Company DUNS | 544349634 |
| Company Name | Safecare Biotech (Hangzhou) Co., Ltd. |
| 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 | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 06974246462608 [Primary] |
| LNW | Paper, Obstetric Ph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-09-26 |
| Device Publish Date | 2025-09-18 |
| 06974246462608 - Safecare Vaginal PH Rapid Test Cassette | 2025-09-26 |
| 06974246462608 - Safecare Vaginal PH Rapid Test Cassette | 2025-09-26 |
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| 06974246462585 - T Testahead HCG Urine Test Strip | 2025-08-28 |
| 06974246462547 - Welcheck HCG Urine Test Midstream | 2025-08-12 |
| 06974246462400 - FIRSTVIEW Luteinizing Hormone Rapid Test Strip | 2025-08-07 |
| 06974246462417 - FIRSTVIEW Luteinizing Hormone Rapid Test Strip | 2025-08-07 |
| 06974246462424 - Exploro Highly Sensitive Urine Drug Test (14-Panel) | 2025-08-07 |
| 06974246462431 - Exploro Highly Sensitive Urine Drug Test (14-Panel) | 2025-08-07 |