Primary Device ID | 00383730003504 |
NIH Device Record Key | d3404464-d7b5-4ae0-95de-5bc78bc2ce24 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | I-neb |
Version Model Number | 00 |
Catalog Number | 1034300 |
Company DUNS | 220018415 |
Company Name | RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD |
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 | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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)387-4000 |
RESPIRONICS.SERVICE@PHILIPS.COM | |
Phone | +1(724)387-4000 |
RESPIRONICS.SERVICE@PHILIPS.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00383730003504 [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 | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-24 |
00383730004396 | I-neb PH Unit Japan |
00383730003931 | I-NEB DISC. |
00383730003832 | I-neb 5.0 Chamber, 2 pack. |
00383730003825 | I-neb 2.5 Chamber, 2 pack. |
00383730003818 | I-neb 0.5 Tidal Breathing MP Chamber Assembly. |
00383730003801 | I-neb Chamber, 0.25 Tested. |
00383730003795 | I-neb Target Inhalation Mode MP. |
00383730003788 | I-neb Tidal Breathing Mode MP. |
00383730003771 | I-neb TBM MouthPiece Assembly Green Dnase Tested. |
00383730003764 | I-neb Chamber, 1.5 Tested. |
00383730003757 | I-neb Chamber, 0.3 Tested. |
00383730003740 | I-neb PH20 Gold Dosing Kit. |
00383730003733 | I-neb Charger. |
00383730003726 | I-neb CF TIM Pack, Europe. |
00383730003719 | I-neb PH Day Kit International Unit. |
00383730003702 | I-neb 5.0 mcg Gold Chamber, 2 pack. |
00383730003696 | I-neb PAH Day Kit US. |
00383730003689 | I-neb TIM MP Grey Chamber Assembly Tested. |
00383730003672 | I-neb TIM MP Lilac Chamber Assembly Tested. |
00383730003665 | I-neb TIM MP Green Chamber Assembly Tested. |
00383730003658 | I-neb Actelion PH 20 Dosing Kit. |
00383730003641 | I-neb Chamber Assembly for Hypertonic Saline. |
00383730003634 | I-neb CF Chamber Assembly Tobramycin. |
00383730003627 | I-neb TIM Mouthpiece Assembly. |
00383730003610 | I-neb Non-Metering TBM M-P White Tested. |
00383730003603 | I-neb Ventavis 5.0 mcg Purple PL6 Disc, US. |
00383730003597 | I-neb Ventavis 2.5 mcg Red Power 6 Disc, US. |
00383730003580 | I-neb Emergency Disc Assembly. |
00383730003573 | I-neb Disc Card Assembly Tadim. |
00383730003566 | I-neb Disc Card Assembly for Promixin. |
00383730003559 | I-neb Ventavis 5.0 mcg Concentrated Dose PL6. |
00383730003542 | I-neb GM-CSF PL15 Disc Assembly. |
00383730003535 | I-neb Emergency Disc Assembly, Blue. |
00383730003528 | I-neb Ventavis 5.0 mcg Purple Disc Assembly |
00383730003511 | I-neb Ventavis 2.5 mcg Red Disc Assembly |
00383730003504 | I-neb Disc Assy, Romedic. |
00383730001005 | I-neb Insight Online Multi-Lang Assembly |
00383730000985 | I-neb PH Australian Unit. |
00383730000978 | I-neb PH USA Unit. |
00383730000961 | I-neb PH UK Unit. |
00383730000954 | I-neb PH Middle East Unit. |
00383730000947 | I-neb CF TBM, TIM Unit Scandinavia. |
00383730000930 | I-neb CF TBM, TIM Unit Central Europe. |
00383730000923 | I-neb Handset Replacement. |
00383730000916 | I-neb CF TBM, TIM, Spain, Portugal Unit. |
00383730000893 | I-neb PH Latin America Unit. |
00383730000886 | I-neb PH Unit Europe South. |
00383730000879 | I-neb PH Unit Europe East. |
00383730000862 | I-neb PH Unit Europe Central. |
00383730000848 | I-neb CF German Unit. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() I-NEB 76613379 3085979 Live/Registered |
RIC Investments, LLC 2004-09-27 |