Primary Device ID | 00744229100102 |
NIH Device Record Key | aed4ae5c-0072-4deb-ae5d-3f7d97b5cfbb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LC Plus |
Version Model Number | 022F81-VP |
Company DUNS | 804736098 |
Company Name | PARI RESPIRATORY EQUIPMENT, INC. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00744229100102 [Package] Contains: 00744229229544 Package: carton [12 Units] In Commercial Distribution |
GS1 | 00744229229544 [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 | 2016-09-30 |
00744229100041 | Mouthpiece, LC Plus |
00744229100102 | Nebulizer Kit, LC Plus, Vios Pro |
00744229100126 | Nebulizer Kit, LC Plus, Retail custom |
00744229100034 | Mouthpiece, LC Plus |
00744229100119 | Nebulizer Kit, LC Plus, custom label |
00744229100089 | LC Plus Neb Set, Ped. Mask |
00744229100072 | LC Plus Neb Set, Adult Mask |
00744229100157 | Baby Neb Set, Sz 2 |
00744229100140 | Baby Neb Set, Sz 1 |
00744229100133 | Baby Neb Set, Sz 0 |
00744229100096 | LC Plus Neb Set |
00744229100720 | PARI LC Plus, Nebulizer Set, PRO |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LC PLUS 74682809 2015017 Live/Registered |
PARI GMBH SPEZIALISTEN FUER EFFEKTIVE INHALATION 1995-06-01 |