| Primary Device ID | 20814434021203 |
| NIH Device Record Key | cd4ff6b5-cc4e-41a2-9180-fa347e87a7b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Getinge Assured Steam Sterilization Indicator |
| Version Model Number | 61301606814 |
| Catalog Number | 61301606814 |
| 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 | 00814434021209 [Primary] |
| GS1 | 10814434021206 [Package] Contains: 00814434021209 Package: Bag [250 Units] In Commercial Distribution |
| GS1 | 20814434021203 [Package] Contains: 10814434021206 Package: Case [16 Units] In Commercial Distribution |
| LRT | Indicator, Sterilization |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-06-18 |
| Device Publish Date | 2019-06-10 |
| 20814434021203 | 61301606814 |
| 20814434021197 | 61301606813 |