Primary Device ID | 10796494005702 |
NIH Device Record Key | e3df23d9-dd65-4509-b74c-89f2a07cb21f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JO - Foil - Classic Hybrid - 5mL - HMC |
Version Model Number | 75008 |
Company DUNS | 067692292 |
Company Name | CC Wellness 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 | 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 |
---|---|
GS1 | 00796494005705 [Primary] |
GS1 | 10796494005702 [Package] Contains: 00796494005705 Package: [350 Units] In Commercial Distribution |
NUC | Lubricant, Personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-10 |
Device Publish Date | 2025-02-28 |
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10796494005702 - JO - Foil - Classic Hybrid - 5mL - HMC | 2025-03-10Water-Based Personal Lubricant |
10796494005702 - JO - Foil - Classic Hybrid - 5mL - HMC | 2025-03-10 Water-Based Personal Lubricant |
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