Primary Device ID | 00663580012025 |
NIH Device Record Key | 78fb32c1-9df9-42d5-89f4-13ab4f192773 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liceguard |
Version Model Number | RobiComb Pro |
Company DUNS | 079196902 |
Company Name | Liceguard, LLC |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00663580012025 [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 | 2023-08-28 |
Device Publish Date | 2023-08-18 |
00663580012025 | RobiComb Pro |
00663580009209 | Egg & Lice Combing Kit |
00663580000800 | No Nit Kit |
00663580000022 | RobiComb |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LICEGUARD 97069950 not registered Live/Pending |
Liceguard, LLC 2021-10-12 |
LICEGUARD 75655964 2416445 Live/Registered |
LICEGUARD, LLC 1999-03-08 |