Primary Device ID | 00854103007042 |
NIH Device Record Key | 5772802d-6555-4cbb-b5a9-aa936b24af80 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LightForce FXi |
Version Model Number | LTC-1500 |
Company DUNS | 858768943 |
Company Name | LITECURE 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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com | |
Phone | 1-877-627-3858 |
customer.service@litecure.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00854103007042 [Primary] |
ILY | Lamp, Infrared, Therapeutic Heating |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2017-07-24 |
00854103007042 | Infrared phototherapy device emitting up to 15 W at 980/810nm in CW or pulsed modes. The device |
00854103007097 | Infrared phototherapy device emitting up to 15 W at 980/810nm in CW or pulsed modes. The device |