Primary Device ID | 04961333240210 |
NIH Device Record Key | 40b33bda-acfe-40fe-b9b0-c1b84c55a1fb |
Commercial Distribution Discontinuation | 2018-03-20 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | VIDEO PROCESSOR |
Version Model Number | EPK-I5010-BR |
Company DUNS | 083211284 |
Company Name | PENTAX OF AMERICA, 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 | 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 | 04961333240210 [Primary] |
PEA | Endoscope, Accessories, Image Post-Processing For Color Enhancement |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2018-03-12 |
04961333244690 | VIDEO PROCESSOR - PTAH (VERSA) |
04961333244607 | VIDEO PROCESSOR - PTAH (VERSA) (USED) |
04961333240234 | VIDEO PROCESSOR (INTERNATIONAL USED) |
04961333240227 | VIDEO PROCESSOR (INTERNATIONAL USED) |
04961333240210 | VIDEO PROCESSOR (BRAZIL USED) |
04961333240203 | VIDEO PROCESSOR (USED) |
04961333240197 | VIDEO PROCESSOR (INTERNATIONAL USED) |
04961333240180 | EPK-1000 VIDEO PROCESSOR (INTERNATIONAL USED) |
04961333232628 | VIDEO PROCESSOR (REFURBISHED) |
04961333232611 | VIDEO PROCESSOR (REFURBISHED) |
04961333232604 | VIDEO PROCESSOR (US USED) |
04961333232598 | VIDEO PROCESSOR (US USED) |
04961333232581 | EPK-1000 VIDEO PROCESSOR (US USED) |
04961333231942 | VIDEO PROCESSOR (US NEW) |
04961333228928 | EPK-1000 VIDEO PROCESSOR (US NEW) |