Primary Device ID | 00815965021669 |
NIH Device Record Key | 1e851528-bf7d-43d9-b6ba-2eaaf937b9c6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pioneer IVF® |
Version Model Number | GPPD-230 |
Catalog Number | GPPD-230 |
Company DUNS | 141732011 |
Company Name | LIFEGLOBAL GROUP, LLC |
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 | false |
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(800)720-6375 |
Sales@LifeGlobal.com | |
Phone | +1(800)720-6375 |
Sales@LifeGlobal.com | |
Phone | +1(800)720-6375 |
Sales@LifeGlobal.com |
Storage Environment Atmospheric Pressure | Between 0.5 KiloPascal and 1.06 KiloPascal |
Storage Environment Atmospheric Pressure | Between 0.5 KiloPascal and 1.06 KiloPascal |
Storage Environment Atmospheric Pressure | Between 0.5 KiloPascal and 1.06 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815965021669 [Primary] |
HHK | CURETTE, SUCTION, ENDOMETRIAL (AND ACCESSORIES) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-21 |
00815965021683 | Propump Single 230V |
00815965021676 | Propump Single 115V |
00815965021669 | Propump Dual 230V |
00815965021652 | Propump Dual 115V |