Primary Device ID | 50833224000533 |
NIH Device Record Key | 40a38fdb-931c-489c-99a7-7a0c1135c9fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sylent |
Version Model Number | SYL211 |
Catalog Number | SYL211 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 800-200-9842 |
customerservice@innomedinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00833224000538 [Primary] |
GS1 | 50833224000533 [Package] Contains: 00833224000538 Package: [32 Units] In Commercial Distribution |
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 |
50833224000540 | Sylent 2 Cushion - MD |
50833224000533 | Sylent 2 Cushion - SM |
50833224000526 | Sylent Nasal Mask - All Sizes Kit |
50833224000519 | Sylent 2 Nasal Mask - MD |
50833224000502 | Sylent 2 Nasal Mask - SM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SYLENT 86751313 5276966 Live/Registered |
American Axle & Manufacturing, Inc. 2015-09-09 |
SYLENT 77802604 3829500 Dead/Cancelled |
RespCare, Inc. 2009-08-12 |
SYLENT 77359506 not registered Dead/Abandoned |
RespCare, Inc. 2007-12-26 |
SYLENT 74333361 1815648 Dead/Cancelled |
Schering Aktiengesellschaft 1992-11-13 |