Primary Device ID | B619K0020C01TA0 |
NIH Device Record Key | a8e1395b-6b63-4447-89c5-837c63665555 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GammaPro Laparoscopic Probe |
Version Model Number | K0020C01 |
Company DUNS | 361955128 |
Company Name | Kubtec |
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 | true |
Manufacturing Date | true |
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 |