Primary Device ID | 08500130070260 |
NIH Device Record Key | c39cdca4-4d0e-4f63-a494-46e03f9566e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Earlens Contact Hearing Solution, Monaural, Left |
Version Model Number | IK01L |
Company DUNS | 611658795 |
Company Name | EARLENS CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | true |
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 |
Handling Environment Atmospheric Pressure | Between 525 Millimeter of Mercury and 795 Millimeter of Mercury |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08500130070260 [Primary] |
PLK | Tympanic Membrane Direct Contact Hearing Aid |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-14 |
Device Publish Date | 2019-05-06 |
08500130070260 | Kit containing Left Ear Tip & Processor Assembly, Left Tympanic Lens, Charger. Processor comes |
00850013007264 | Kit containing Left Ear Tip & Processor Assembly, Left Tympanic Lens, Charger. Processor comes |