Primary Device ID | 00860009695214 |
NIH Device Record Key | c3d7bf62-edf8-4941-aa53-728897da4776 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Innara Health |
Version Model Number | IN-5001 |
Catalog Number | IN-5001 |
Company DUNS | 809608719 |
Company Name | INNARA HEALTH, INC. |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00860009695214 [Primary] |
HCC | Device, biofeedback |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-02-02 |
Device Publish Date | 2022-11-03 |
10196852668189 | Patient Consumables (box of 10) |
10196852173638 | Handpiece Tubing, NTrainer System 2.0 (Qty 2) |
00196852125432 | Handpiece, NTrainer System 2.0 (Qty 1) |
00196852124213 | NTrainer System 2.0 |
10860009695266 | Wee Soothies, Purple (box of 20) |
10860009695259 | NICU Soothies, Green (box of 20) |
10860009695242 | Patient Consumables (box of 20) |
10860009695235 | Patient Consumables (box of 10) |
10860009695228 | Handpiece Tubing, NTrainer System 2.0 (Qty 2) |
00860009695214 | Handpiece, NTrainer System 2.0 (Qty 1) |
00860009695207 | NTrainer System 2.0 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INNARA HEALTH 86111397 4563218 Live/Registered |
Innara Health, Inc. 2013-11-06 |
INNARA HEALTH 85809195 4602192 Live/Registered |
INNARA HEALTH, INC. 2012-12-21 |