| Primary Device ID | 00686209100910 |
| NIH Device Record Key | 25746602-38d5-4f2c-857a-1222dad9ecea |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Apilus |
| Version Model Number | CLEO BLEND 256 |
| Catalog Number | 01-0091US |
| Company DUNS | 246237945 |
| Company Name | Dectro International |
| 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 | true |
| 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 | 00686209100910 [Primary] |
| KCW | Epilator, High Frequency, Needle-Type |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-31 |
| Device Publish Date | 2024-05-23 |
| 00686209101238 | needle-type epilator |
| 00686209106059 | needle-type epilator |
| 00686209106004 | needle-type epilator |
| 00686209101115 | needle-type epilator |
| 00686209100910 | needle-type epilator |
| 00686209100903 | needle-type epilator |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() APILUS 86200266 4636121 Live/Registered |
Dectronique 1984 inc. 2014-02-21 |
![]() APILUS 77077972 not registered Dead/Abandoned |
DECTRONIQUE 1984 INC. 2007-01-08 |