Primary Device ID | 00383730002156 |
NIH Device Record Key | 6f3bb044-0cd7-48ec-b792-0c9b5840d7ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InnoSpire Mini |
Version Model Number | 00 |
Catalog Number | 1115507 |
Company DUNS | 220018415 |
Company Name | RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD |
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 | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com | |
Phone | +1(724)744-2500 |
respironics.service@philips.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00383730002156 [Primary] |
CAF | NEBULIZER (DIRECT PATIENT INTERFACE) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-24 |
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