Primary Device ID | D724P2309141 |
NIH Device Record Key | cad1a002-bbd0-4819-b78e-2a7f2f7bffd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PQ Autoclave Pouches (12" x 15") Blue Film (200) |
Version Model Number | P23-0914 |
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 | D724P2309141 [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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