| Primary Device ID | 00724995220273 | 
| NIH Device Record Key | 8a634207-3e57-4072-ad15-5c8fa1ba8e92 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Version Model Number | Quick Connect | 
| Catalog Number | QFC1801E | 
| Company DUNS | 868205779 | 
| Company Name | STERIS CORPORATION | 
| 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 | false | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | false | 
| OTC Over-The-Counter | true | 
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | |
| Phone | +1(800)548-4873 | 
| xx@xx.xx | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00724995220273 [Primary] | 
| MED | Sterilant, medical devices | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2023-10-31 | 
| Device Publish Date | 2023-01-09 | 
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