Primary Device ID | 00851607003167 |
NIH Device Record Key | 25752575-dd4c-4a02-9c5e-a5b1a0eeffe3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Assy, Philips 23' Pulmo Chest Bellows, Tubing ES |
Version Model Number | 459800663242 |
Company DUNS | 962187964 |
Company Name | MEDSPIRA, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com | |
Phone | 612-789-0013 |
info@medspira.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851607003167 [Primary] |
GS1 | 10851607003164 [Package] Package: Shipper [1 Units] In Commercial Distribution |
GS1 | 10851607003168 [Package] Package: Shipper [1 Units] Discontinued: 2018-01-16 Not in Commercial Distribution |
HCC | Device, Biofeedback |
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 | 2017-09-20 |