Primary Device ID | 04032767084494 |
NIH Device Record Key | 61e064d2-d918-40ac-8c2e-580dce74d7fc |
Commercial Distribution Discontinuation | 2020-03-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Electrode Accessories |
Version Model Number | 13E153 |
Company DUNS | 300802068 |
Company Name | Otto Bock Healthcare Products GmbH |
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 | false |
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 |