Primary Device ID | 00814005021584 |
NIH Device Record Key | 8e615e86-e202-4740-86a2-673e6373f2d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 14P1 |
Version Model Number | 14P1 |
Catalog Number | 300-10123 |
Company DUNS | 121431159 |
Company Name | Quality Aspirators, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814005021584 [Primary] |
EHZ | Evacuator, oral cavity |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-07 |
Device Publish Date | 2025-02-27 |
00814005020006 - TA | 2025-03-07 TA |
00814005020013 - 15P2-90A | 2025-03-07 15P2-90A |
00814005020037 - 03BAT | 2025-03-07 03BAT |
00814005020051 - 15P3A | 2025-03-07 15P3A |
00814005020068 - 03BA | 2025-03-07 03BA |
00814005020082 - 02BA | 2025-03-07 02BA |
00814005020099 - 46P3M | 2025-03-07 46P3M |
00814005020105 - 15P2AT | 2025-03-07 15P2AT |