| Primary Device ID | 00862572000358 |
| NIH Device Record Key | 29294564-fcc6-479a-8462-d64d9b2b2dbf |
| Commercial Distribution Discontinuation | 2099-05-07 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Westcliff Medical Products |
| Version Model Number | WC6018 |
| Company DUNS | 067695404 |
| Company Name | WESTCLIFF MEDICAL PRODUCTS |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00862572000358 [Primary] |
| GS1 | 10862572000355 [Package] Package: Box [200 Units] Discontinued: 2099-05-07 In Commercial Distribution |
| GS1 | 20862572000352 [Package] Contains: 10862572000355 Package: Case [800 Units] Discontinued: 2099-05-07 In Commercial Distribution |
| KST | System, Blood Collection, Vacuum-Assisted, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-27 |
| Device Publish Date | 2019-05-17 |