Primary Device ID | 50833224000212 |
NIH Device Record Key | 14d4885a-a93a-43c2-845f-9d3beb9aa656 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hybrid |
Version Model Number | HYB521 |
Catalog Number | HYB521 |
Company DUNS | 103307950 |
Company Name | Innomed Technologies 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 | true |
Serial Number | false |
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 |
Phone | 800-200-9842 |
customerservice@innomedinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00833224000217 [Primary] |
GS1 | 50833224000212 [Package] Contains: 00833224000217 Package: [96 Units] In Commercial Distribution |
HIBCC | M694HYB5211 [Secondary] |
BZD | Ventilator, Non-Continuous (Respirator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-15 |
50833224001196 | Hybrid Frame System - LG |
50833224001189 | Hybrid Frame System - MD |
50833224001172 | Hybrid Frame System - SM |
50833224001165 | Hybrid Frame System - All Sizes Kit |
50833224000236 | Hybrid SLV Face Mask – All Sizes Kit |
50833224000212 | Hybrid Pillows - SM |
50833224000205 | Hybrid Pillows - MD |
50833224000199 | Hybrid Pillows - LG |
50833224000182 | Hybrid Cushion- SM |
50833224000175 | Hybrid Cushion- MD |
50833224000168 | Hybrid Cushion- LG |
50833224000151 | Hybrid Face Mask - All Sizes Kit |