Primary Device ID | B362101271 |
NIH Device Record Key | 44f596c9-78ad-4c00-9e04-7edebe86f4f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JO Premium Original 1oz/30ml |
Version Model Number | 10127 |
Company DUNS | 067692292 |
Company Name | United Consortium |
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 | 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 | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B362101270 [Primary] |
HIBCC | B362101271 [Package] Contains: B362101270 Package: [24 Units] In Commercial Distribution |
NUC | Lubricant, Personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2018-05-21 |
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