Primary Device ID | 00606959026742 |
NIH Device Record Key | 3ca76de6-74a1-4445-b8da-e51bc185d7f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WISP PEDIATRIC |
Version Model Number | 00 |
Catalog Number | 1104965 |
Company DUNS | 080728314 |
Company Name | Respironics, 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 | true |
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 |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Storage Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Storage Environment Temperature | Between -4 Degrees Fahrenheit and 140 Degrees Fahrenheit |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00606959026742 [Primary] |
BZD | VENTILATOR, NON-CONTINUOUS (RESPIRATOR) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-03-01 |
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00606959026742 | WISP PED FIT PACK wHEADGEAR - EE JPN |
00606959026728 | Wisp Ped VIP Fit Pack - EE |