Primary Device ID | 47290013484688 |
NIH Device Record Key | 71b7f369-1d6f-4622-849f-7ff2bb2d5028 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spike Tubing EZ |
Version Model Number | SA-EZ/E |
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 | 07290013484680 [Primary] |
GS1 | 27290013484684 [Package] Contains: 07290013484680 Package: Case [60 Units] In Commercial Distribution |
GS1 | 47290013484688 [Package] Contains: 07290013484680 Package: Box [15 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 | 2024-06-14 |
Device Publish Date | 2024-06-06 |
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 | 2024-06-14Tubing Sets |
47290013484688 - Spike Tubing EZ | 2024-06-14 Tubing Sets |
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 |