Primary Device ID | 00858526006729 |
NIH Device Record Key | 894a4aeb-a9e0-4430-8f2e-bfcdecab5a30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRC |
Version Model Number | 19233-84 |
Company DUNS | 080143399 |
Company Name | PRENTKE ROMICH COMPANY |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | true |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com | |
Phone | 800-262-1984 |
info@prentrom.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858526006729 [Primary] |
ILQ | System, Communication, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
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