Primary Device ID | 00810061048145 |
NIH Device Record Key | 731e5df6-f915-4733-b47d-fe2cf023277e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RID |
Version Model Number | 02100297/80014X |
Company DUNS | 117628199 |
Company Name | Oystershell Consumer Health, Inc |
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 | true |
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 | 00810061048145 [Primary] |
LJL | Detectors And Removers, Lice, (Including Combs) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-03 |
Device Publish Date | 2022-09-23 |
00810061048282 | Super Max Sensitive Skin Lice Elimination Kit |
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00810061048268 | Super Max Complete Lice Elimination Kit |
00810061048145 | Super Max Sensitive Skin Lice Elimination Kit |
00810061048138 | Super Max Complete Lice Elimination Kit |
00810061048114 | Super Max Lice Elimination Kit |