Primary Device ID | 08717524640064 |
NIH Device Record Key | f86f66c8-1cbf-4245-9ce0-c0f256bf2a90 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lode B.V. |
Version Model Number | 938900 |
Company DUNS | 407774181 |
Company Name | Lode B.V. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 08717524640064 [Primary] |
IOL | TREADMILL, POWERED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2017-05-09 |
08717524640170 | 934900 Katana sport |
08717524640163 | 934930 Katana sport XL |
08717524640156 | 938902 Valiant 2 sport |
08717524640118 | 938906 Valiant 2 sport XL |
08717524640101 | 938905 Valiant 2 cpet XL |
08717524640095 | 938904 Valiant 2 pediatric |
08717524640088 | 938903 Valiant 2 rehab XL |
08717524640071 | 938901 Valiant 2 rehab |
08717524640064 | 938900 Valiant 2 cpet |