Primary Device ID | 00850071887242 |
NIH Device Record Key | 37809bd7-abcb-4f28-9c3d-a0594e0e6e9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Emergent Respiratory |
Version Model Number | 1900-001 |
Company DUNS | 117921082 |
Company Name | MDL Solutions Incorporated |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com | |
Phone | 6125427979 |
help@emergentcpap.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850071887242 [Primary] |
BTL | Ventilator, Emergency, Powered (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-14 |
Device Publish Date | 2025-04-05 |
00850071887242 | PortO2 Vent CPAP |
00850071887174 | Breathing Circuit with Large S3 Mask |
00850071887136 | Breathing Circuit with Small S3 Mask |
00850071887013 | Breathing Circuit with Medium S3 Mask |