Primary Device ID | 00856096008297 |
NIH Device Record Key | 2061bcdd-7d82-46b1-b253-a5d8884520a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anybattery |
Version Model Number | 4456-2 |
Catalog Number | 4456-2 |
Company DUNS | 005272799 |
Company Name | ANYBATTERY, 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 | true |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00856096008297 [Primary] |
MOQ | Battery, Replacement, Rechargeable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-05-17 |
Device Publish Date | 2019-05-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANYBATTERY 85351766 4090899 Live/Registered |
ANYBATTERY INC 2011-06-21 |
ANYBATTERY 75692978 2557661 Dead/Cancelled |
Steddy, Inc. 1999-04-28 |
ANYBATTERY 75680695 not registered Dead/Abandoned |
NETNEWBUSINESS, INC. 1999-04-12 |