Primary Device ID | 00383730004365 |
NIH Device Record Key | e60c7f50-bec3-4deb-87d0-7fa34f2e5e0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | System 22 |
Version Model Number | 00 |
Catalog Number | 1025529 |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(724)744-2500 |
RESPIRONICS.SERVICE@PHILIPS.COM | |
Phone | +1(724)744-2500 |
RESPIRONICS.SERVICE@PHILIPS.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00383730004365 [Primary] |
BYG | MASK, OXYGEN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-06-11 |
Device Publish Date | 2017-08-30 |
00383730004365 | MASK - SIDESTREAM PEDIATRIC |
00383730004327 | SIDESTREAM TUCKER THE TURTLE MASK BX=50E |
00383730004280 | SYSTEM 22 SYSTEM MASK PEDIATRIC-50CS |
00383730004273 | ADULT SYSTEM AEROSOL MASK -100CS |
00383730004266 | CHILD SYSTEM AEROSOL MASK (EACH) |
00383730004259 | SYSTEM 22 PEDIATRIC AEROSOL MSK SUB ASSY |
00383730004242 | SYS 22 ADULT MASK-50CS |
00383730004235 | ADULT SYSTEM AEROSOL MASK (EACH) |
00383730004211 | SYSTEM 22 ADULT AEROSOL MASK ASSEMBLY |
00383730003948 | MASK - SIDESTREAM ADULT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SYSTEM 22 73618471 1545869 Dead/Cancelled |
MEDIC-AID LIMITED 1986-09-08 |