Primary Device ID | 00036000623550 |
NIH Device Record Key | 31ed0043-3e0d-44be-92c7-b5f691a15c54 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KIMBERLY-CLARK® PFR95™ N95 Particulate Filter Respirator and Surgical Mask |
Version Model Number | 62355 |
Company DUNS | 830997032 |
Company Name | KIMBERLY-CLARK GLOBAL SALES, LLC |
Device Count | 50 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(888)346-4652 |
xxx@xxx.xxx |
Special Storage Condition, Specify | Between 0 and 0 *Protect from sources of light and radiation; Protect from moisture. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00036000623550 [Primary] |
GS1 | 10036000623557 [Package] Package: Case [6 Units] In Commercial Distribution |
GS1 | 90036000623553 [Unit of Use] |
MSH | Respirator,surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2016-11-30 |
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