Anybattery 3394
GUDID 00856096008013
12v / SLA
ANYBATTERY, INC
Rechargeable battery pack| Primary Device ID | 00856096008013 |
| NIH Device Record Key | e1b69a22-2559-452c-a107-47b615561e1e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Anybattery |
| Version Model Number | 3394 |
| Catalog Number | 3394 |
| Company DUNS | 005272799 |
| Company Name | ANYBATTERY, 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 | false |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00856096008013 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K160667
FDA Product Code
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) |
| MOX | Batteries, Rechargeable, For Class 2 Devices |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-21 |
| Device Publish Date | 2019-01-21 |
On-Brand Devices [Anybattery]
Trademark Results [Anybattery]
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 |
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