Primary Device ID | B1824727TG70503 |
NIH Device Record Key | 3384b8c7-942b-4396-9e17-52d77b5337b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CapnoVue |
Version Model Number | 1002-A 4727TG-7-0-50 |
Company DUNS | 022721133 |
Company Name | SALTER LABS |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1 (425) 406-6235 |
support@monitormask.com | |
Phone | +1 (425) 406-6235 |
support@monitormask.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B1824727TG700 [Primary] |
HIBCC | B1824727TG70503 [Package] Contains: B1824727TG700 Package: Shipper Box [50 Units] In Commercial Distribution |
BYG | Mask, Oxygen |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-06-19 |
Device Publish Date | 2018-12-17 |
B1824737TG70503 | 2002-A 4737TG-7-0-50 |
B1824737140503 | 2004-A 4737-14-0-50 |
B1824727TG70503 | 1002-A 4727TG-7-0-50 |
B18247271400 | 1004-A 4727-14-0-50 |
B1822001P0 | 2001-P |
B1822001A503 | 2001-A |
B1821001P503 | 1001-P |
B1821001I0 | 1001-I |
B1821001A0 | 1001-A |
10607411971393 | CapnoVue Scope O2/CO2 Mask with reflective connector |
10607411971386 | CapnoVue Scope O2/CO2 Mask with reflective connector |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CAPNOVUE 86561248 4984574 Live/Registered |
Monitor Mask Inc. 2015-03-11 |