MASK - OC ADV HS81211-010

GUDID 00383730001173

OC Advanced Pediatric Medium Mask

RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD

Medicine chamber spacer, reusable
Primary Device ID00383730001173
NIH Device Record Keyc0a75369-3210-4c17-8c9c-72e28509663e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMASK - OC ADV
Version Model Number00
Catalog NumberHS81211-010
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 Kitfalse
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
GS100383730001173 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CAFNEBULIZER (DIRECT PATIENT INTERFACE)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-24

Devices Manufactured by RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD

00383730004648 - OVAL MOUTHPIECE2020-06-19 OVAL MOUTHPIECE
00383730004624 - PLASTIC PEDIATRIC MOUTHPIECES (715)100PK2020-06-17 PLASTIC PEDIATRIC MOUTHPIECES (715)100PK
00383730004631 - PLASTIC PEDIATRIC DISPOSABLE MOUTHPIECE2020-06-17 PLASTIC PEDIATRIC DISPOSABLE MOUTHPIECE
00383730004617 - OVAL DISPOSABLE PLASTIC MOUTHPIECE2020-06-15 OVAL DISPOSABLE PLASTIC MOUTHPIECE
00383730004495 - TBM MP Gold Chamber Assy Tested2020-04-01 Tidal Breathing Mode Mouthpiece Gold Chamber Assembly Tested
00383730004501 - I-neb Clinical Study Disc2020-04-01 I-neb Clinical Study Disc
00383730004518 - I-neb Generic ClinicalStudy Disc Power102020-04-01 I-neb Generic Clinical Study Disc Power10
00383730004587 - I-neb In Vitro Test Disc Power 102020-04-01 I-neb In Vitro Test Disc Power 10

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