Primary Device ID | 00689519011105 |
NIH Device Record Key | f20e0ce9-8489-468e-b089-6b043bb1f87a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pumpmatic |
Version Model Number | 110 |
Company DUNS | 007176126 |
Company Name | Ashton Pumpmatic, Inc. |
Device Count | 25 |
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 | 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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00689519001106 [Primary] |
GS1 | 00689519003100 [Primary] |
GS1 | 00689519011105 [Unit of Use] |
GGY | PIPETTE, DILUTING |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-22 |
Device Publish Date | 2023-12-14 |
00689519017015 | 701 |
00689519012102 | 210 |
00689519012058 | 205 |
00689519012010 | 201 |
00689519011105 | 110 |
00689519011051 | 105 |
00689519011013 | 101 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PUMPMATIC 97558018 not registered Live/Pending |
BRS BATTERY LTD. 2022-08-22 |
PUMPMATIC 73670663 1478527 Dead/Expired |
ASHTON INDUSTRIES, INC. 1987-07-02 |