| Primary Device ID | 47290013484749 |
| NIH Device Record Key | 224cf7ab-06d8-47c9-bb99-e2703d15cc4c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Luer Lock Adaptor 2 A |
| Version Model Number | LL-2A |
| Company DUNS | 533172743 |
| Company Name | EQUASHIELD MEDICAL 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290013484741 [Primary] |
| GS1 | 27290013484745 [Package] Contains: 07290013484741 Package: Case [480 Units] In Commercial Distribution |
| GS1 | 47290013484749 [Package] Contains: 07290013484741 Package: Box [120 Units] In Commercial Distribution |
| ONB | Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-20 |
| Device Publish Date | 2024-03-12 |
| 47290013484664 - Spike Adaptor EZ | 2024-10-18 |
| 47290013484671 - Spike Adaptor EZ Dual | 2024-10-18 |
| 47290013484763 - Spike Adaptor EZ W | 2024-10-18 |
| 47290013484688 - Spike Tubing EZ | 2024-06-14 Tubing Sets |
| 47290013484749 - Luer Lock Adaptor 2 A | 2024-03-20 |
| 47290013484749 - Luer Lock Adaptor 2 A | 2024-03-20 |
| 47290013484756 - Luer Lock Adaptor 2 Swivel A | 2024-03-20 |
| 47290013484695 - Secondary Tubing EZ | 2023-10-26 |
| 17290013484656 - Equashield | 2022-08-02 Luer Lock Adaptor Swivel |