Primary Device ID | 10031262094381 |
NIH Device Record Key | f35e8c8a-1080-484a-a777-4d5f3b80ac5d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BROOKSTONE |
Version Model Number | B-HHP-640J |
Company DUNS | 183280973 |
Company Name | FKA DISTRIBUTING CO., LLC |
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 | 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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00031262094384 [Primary] |
GS1 | 10031262094381 [Package] Contains: 00031262094384 Package: Case [4 Units] In Commercial Distribution |
ISA | Massager, Therapeutic, Electric |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
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