Primary Device ID | 04560141945166 |
NIH Device Record Key | 1dfea789-7e52-493f-bb81-89acf025d7fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CS-7 |
Version Model Number | A4C1 |
Company DUNS | 692076161 |
Company Name | KONICA MINOLTA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04560141945166 [Primary] |
LLZ | System, Image Processing, Radiological |
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 | 2016-09-19 |
04560141951433 - Bone Suppression Software | 2024-07-16 |
04560141950399 - ImagePilot | 2023-07-27 |
04560141950771 - G-59 | 2023-06-22 |
04560141950788 - G-60 | 2023-06-22 |
04560141950795 - G-22 | 2023-06-22 |
04560141950849 - KONICAMINOLTA DI-X1 | 2023-05-12 |
04560141949287 - P-65 | 2022-11-25 |
04560141949294 - P-75 | 2022-11-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CS-7 73801805 1611869 Dead/Cancelled |
PILKINGTON VISIONCARE, INC. 1989-05-22 |