Primary Device ID | 07613327419153 |
NIH Device Record Key | 872ff654-947a-4fb4-adda-57db0c8032c7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Connected OR HUB |
Version Model Number | 0240200103 |
Catalog Number | 0240200103 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
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 | true |
OTC Over-The-Counter | false |