Primary Device ID | 07640161461055 |
NIH Device Record Key | 6dbf84ab-0a9e-4dd4-8b38-b6095e200ea7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BEMER Therapy Systems |
Version Model Number | Professional |
Catalog Number | 410201 |
Company DUNS | 448002860 |
Company Name | Bemer Int. AG |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640161461055 [Primary] |
GS1 | 07640161461062 [Package] Package: [1 Units] In Commercial Distribution |
GS1 | 07640161461079 [Package] Package: [1 Units] In Commercial Distribution |
GS1 | 07640161462038 [Package] Package: [1 Units] In Commercial Distribution |
NGX | Stimulator, Muscle, Powered, For Muscle Conditioning |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-28 |
Device Publish Date | 2017-05-03 |
07640161461048 | B.BOX Professional |
07640161461017 | B.BOX Classic |
07640161461055 | Professional |