| Primary Device ID | D724P2301461 | 
| NIH Device Record Key | 5a79ee5a-8392-49a1-9419-176090a8776a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | PQ Autoclave Pouches (2-1/4" x 5") Blue Film (200) | 
| Version Model Number | P23-0146 | 
| Company DUNS | 082874108 | 
| Company Name | PEARSON DENTAL SUPPLIES, 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 | true | 
| Device Combination Product | false | 
| Single Use | true | 
| 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 | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | D724P2301461 [Primary] | 
| FRC | Indicator, Biological Sterilization Process | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2019-11-08 | 
| Device Publish Date | 2016-08-22 | 
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