ProChamber Assembly 1117488

GUDID 00383730000688

PROCHAMBER WITH LARGE SILICONE MASK 50-pack

RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD

Medicine chamber spacer, reusable
Primary Device ID00383730000688
NIH Device Record Key8bcf9542-b39d-4369-9afc-7be0bc77ebc4
Commercial Distribution StatusIn Commercial Distribution
Brand NameProChamber Assembly
Version Model Number00
Catalog Number1117488
Company DUNS220018415
Company NameRESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com
Phone+1(724)744-2500
Emailrespironics.service@philips.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100383730000688 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BWFSPIROMETER, THERAPEUTIC (INCENTIVE)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-11-12
Device Publish Date2016-08-24

On-Brand Devices [ProChamber Assembly]

00383730000718PROCHAMBER VHC - 50PK
00383730000701PROCHAMBER WMEDIUM SILICONE MASK 50-pack
00383730000695PROCHAMBER WITH SMALL SILICONE MASK 50-pack
00383730000688PROCHAMBER WITH LARGE SILICONE MASK 50-pack
00383730000671PROCHAMBER RETAIL - 10PK
00383730000664PROCHAMBER SPAIN - 10PK
00383730000657ProChamber Assembly

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.