Primary Device ID | 00850025688819 |
NIH Device Record Key | 3f99333d-a747-4f9f-86bd-9cd9f9f15ff9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | myPKFiT for Healthcare Professionals |
Version Model Number | V3 |
Company DUNS | 041877817 |
Company Name | Takeda Pharmaceuticals U.S.A., 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 | false |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850025688819 [Primary] |
PHY | Sparse Sample Pk Profile And Dosing Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-13 |
Device Publish Date | 2025-01-03 |
00850025688819 - myPKFiT for Healthcare Professionals | 2025-01-13Web application used by Healthcare Professionals to generate dose calculations |
00850025688819 - myPKFiT for Healthcare Professionals | 2025-01-13 Web application used by Healthcare Professionals to generate dose calculations |
00850025688826 - myPKFiT for Patients Mobile Application | 2025-01-13 Mobile application used by patients for disease management |
00850025688871 - BAXJECT II Hi-Flow | 2024-06-20 Needleless Transfer Device |
00850025688864 - BAXJECT II | 2024-03-08 Needleless Transfer Device |
00850025688888 - Anti-Drug Antibody Biomarker Specimen Collection Kit | 2023-11-07 The purpose of the Anti-Drug Antibody and Biomarker Specimen Collection Kit is to aid healthcare providers (HCPs) in collectings |