| Primary Device ID | 00860001024012 |
| NIH Device Record Key | 15de693b-1af0-4748-a253-fe2525230d2e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 75mm Hemato-clad Heparinized |
| Version Model Number | 1-000-7500-HC |
| Catalog Number | 1-000-7500-HC/5 |
| Company DUNS | 002354272 |
| Company Name | DRUMMOND SCIENTIFIC COMPANY |
| Device Count | 5 |
| 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 | false |
| Phone | +1(215)441-6438 |
| GFalatovich@reedtech.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860001024012 [Primary] |
| GS1 | 10860001024019 [Unit of Use] |
| GHY | HEMATOCRIT, TUBE, RACK, SEALER, HOLDER |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-05-09 |
| Device Publish Date | 2019-05-01 |
| 00860001024050 - MICROSAFE | 2025-05-14 MICROSAFE, 35 ul |
| 00850059420355 - SAFECAP | 2024-05-27 SAFECAP, Heparanized |
| 00850059420362 - SAFECAP | 2024-05-27 SAFECAP, Plain |
| 00850059420379 - SAFECAP | 2024-05-27 SAFECAP, Precalibrated |
| 00850059420249 - MICROSAFE | 2024-05-27 MICROSAFE, 5 ul |
| 00850059420232 - MICROSAFE | 2024-05-27 MICROSAFE, 10 ul short |
| 00850059420225 - MICROSAFE | 2024-05-27 MICROSAFE, 15 ul |
| 00850059420348 - MICROSAFE | 2024-05-27 MICROSAFE, 17 ul |