Primary Device ID | 00848657077729 |
NIH Device Record Key | ceb0e7ae-9d39-4ab2-905e-57b3191db573 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AED ENDOPRO® PRIMO SERIES CAMERA |
Version Model Number | EP2050HD |
Company DUNS | 839138955 |
Company Name | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | false |
OTC Over-The-Counter | false |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md | |
Phone | 8182272720 |
customerservice@aed.md |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00848657077729 [Primary] |
FWF | Camera, Television, Endoscopic, Without Audio |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-10-03 |
Device Publish Date | 2025-09-25 |
00848657077088 | AED ENDOPRO® PRIMO SERIES CAMERA |
00848657077729 | AED ENDOPRO® PRIMO SERIES CAMERA |