Assy, Philips 23' Pulmo Chest Bellows, Tubing ES

GUDID 00851607003167

Custom Assembly. Philips 23" Pulmo Chest Bellows, Tubing ES

MEDSPIRA, LLC

Breath-hold system patient belt, pneumatic
Primary Device ID00851607003167
NIH Device Record Key25752575-dd4c-4a02-9c5e-a5b1a0eeffe3
Commercial Distribution StatusIn Commercial Distribution
Brand NameAssy, Philips 23' Pulmo Chest Bellows, Tubing ES
Version Model Number459800663242
Company DUNS962187964
Company NameMEDSPIRA, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com
Phone612-789-0013
Emailinfo@medspira.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100851607003167 [Primary]
GS110851607003164 [Package]
Package: Shipper [1 Units]
In Commercial Distribution
GS110851607003168 [Package]
Package: Shipper [1 Units]
Discontinued: 2018-01-16
Not in Commercial Distribution

FDA Product Code

HCCDevice, Biofeedback

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-09-20