Primary Device ID | 00810170018848 |
NIH Device Record Key | 82194e6b-f8f6-4ddc-93e6-c8f6073c8d96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ERIC Retrieval Device |
Version Model Number | ER174030-US |
Catalog Number | ERIC174030 |
Company DUNS | 003263105 |
Company Name | MICROVENTION 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810170018848 [Primary] |
NRJ | Ultrasound, skin permeation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-20 |
Device Publish Date | 2022-10-12 |
00810170018862 | ERIC 6 |
00810170018848 | ERIC 4 |
00810170018831 | ERIC 3 |