Primary Device ID | 06973071102000 |
NIH Device Record Key | 2a026eba-a48e-4ba7-a2a7-68acc4acaf08 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hand-held IPL device (IPL Home Use Hair Removal Device) |
Version Model Number | FZ-200 |
Company DUNS | 707411576 |
Company Name | Shenzhen IONKA Medical Technology Co., Ltd. |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973071102000 [Primary] |
OHT | Light Based Over-The-Counter Hair Removal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-09 |
Device Publish Date | 2023-08-01 |
06973071106183 | IPL Home Use Hair Removal Device is indicated for the removal of unwanted hair. The device is al |
06973071106084 | IPL Home Use Hair Removal Device is indicated for the removal of unwanted hair. The device is al |
06973071102000 | IPL Home Use Hair Removal Device is indicated for the removal of unwanted hair. The device is al |
06973071101003 | IPL Home Use Hair Removal Device is indicated for the removal of unwanted hair. The device is al |