| Primary Device ID | 20814434020565 |
| NIH Device Record Key | ff0a9830-941c-4bfe-aded-ddcd77990909 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SteriTec Migrating Integrator |
| Version Model Number | CI 163 |
| Catalog Number | CI 163, CI 163/250 |
| Company DUNS | 622223196 |
| Company Name | STERITEC PRODUCT MFG. CO., INC. |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814434020561 [Primary] |
| GS1 | 10814434020568 [Package] Contains: 00814434020561 Package: Bag [1000 Units] In Commercial Distribution |
| GS1 | 20814434020565 [Package] Contains: 10814434020568 Package: Case [12 Units] In Commercial Distribution |
| GS1 | 30814434020562 [Package] Contains: 00814434020561 Package: Bag [250 Units] In Commercial Distribution |
| GS1 | 40814434020569 [Package] Contains: 30814434020562 Package: Case [48 Units] In Commercial Distribution |
| JOJ | Indicator, Physical/Chemical Sterilization Process |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |