Primary Device ID | 00850005738268 |
NIH Device Record Key | 6a3b676d-a2ff-4d5e-bbc1-5c2fadd260f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRIMUS Steam Sterilizer |
Version Model Number | PSS11-HB |
Company DUNS | 825069404 |
Company Name | Primus Sterilizer Company, LLC |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx | |
Phone | 4023444200 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850005738268 [Primary] |
FLE | Sterilizer, Steam |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-23 |
Device Publish Date | 2024-05-15 |
00850005738268 | PRIMUS Steam Sterilizer ,Healthcare (Model PSS11-HB) |
00850005738251 | PRIMUS Steam Sterilizer ,Healthcare (Model PSS11-HA) |