| Primary Device ID | 20888937000614 |
| NIH Device Record Key | 821088cf-e665-4c27-bb3f-26976d3d4bf8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Handyvak Locking Syringe |
| Version Model Number | MX500 |
| Company DUNS | 801895244 |
| Company Name | Coopersurgical, 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 | 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888937000610 [Primary] |
| GS1 | 20888937000614 [Package] Contains: 00888937000610 Package: [10 Units] In Commercial Distribution |
| FMF | Syringe, Piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-18 |
| 00888937028126 - Biopsy Medium | 2026-02-12 Biopsy Medium. 10 ml |
| 00888937028157 - Sperm Freezing Medium | 2026-02-12 Sperm Freezing Medium. 10ml |
| 00888937028218 - PVP Medium | 2026-02-12 PVP Medium with phenol red. 1 ml |
| 60888937028272 - Universal IVF Medium | 2026-02-12 Universal IVF Medium. 60 ml |
| 00888937028287 - Universal IVF Medium | 2026-02-12 Universal IVF Medium with phenol red. 60 ml |
| 00888937028317 - UTM | 2026-02-12 UTM Transfer Medium with phenol red. 10 ml |
| 00888937028324 - UTM | 2026-02-12 UTM Transfer Medium |
| 00888937028577 - Flushing Medium | 2026-02-12 Flushing Medium without Heparin. 125 ml |