| Primary Device ID | 35020583123206 |
| NIH Device Record Key | 93ec502a-7f07-4608-8a09-c2592b3ae64d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Spectra Optia IDL Set |
| Version Model Number | 12320 |
| Company DUNS | 801679200 |
| Company Name | TERUMO BCT, INC. |
| Device Count | 6 |
| DM Exempt | true |
| 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 | true |
| 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 |
| Phone | +1(303)205-2510 |
| FDAUDIprogram@terumobct.com | |
| Phone | +1(303)205-2510 |
| FDAUDIprogram@terumobct.com |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from rain |
| Storage Environment Temperature | Between 0 Degrees Celsius and 35 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of sunlight. |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from rain |
| Storage Environment Temperature | Between 0 Degrees Celsius and 35 Degrees Celsius |
| Special Storage Condition, Specify | Between 0 and 0 *Keep out of sunlight. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05020583123205 [Unit of Use] |
| GS1 | 35020583123206 [Primary] |
| GKT | Separator, automated, blood cell, diagnostic |
| 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 | 2016-09-15 |
| 35020583123206 | Spectra Optia IDL Set |
| 35020583103109 | Spectra Optia IDL Set |
| 35020583103000 | Spectra Optia IDL Set |