Primary Device ID | 00260720011353 |
NIH Device Record Key | 402dc327-e87f-4619-8f8e-a769dedadbe3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Drager |
Version Model Number | L049-700-010 |
Catalog Number | L049-700-010 |
Company DUNS | 099674145 |
Company Name | ALLIED HEALTHCARE PRODUCTS, 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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
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 | 00260720011353 [Primary] |
BTA | Pump, Portable, Aspiration (Manual Or Powered) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-16 |
00260720011353 | Aspirator |
00026072011355 | Aspirator |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DRAGER 73623646 1582085 Live/Registered |
DRAGERWERK AG 1986-10-02 |