| Primary Device ID | D724P2301471 |
| NIH Device Record Key | e485d98f-edce-443e-97b7-d838655e35da |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PQ Autoclave Pouches (7" x 12") Blue Film (100) |
| Version Model Number | P23-0147 |
| 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 | D724P2301471 [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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