Primary Device ID | 08592346848986 |
NIH Device Record Key | 6cf0b292-ee39-4e7e-899a-d0740298faa8 |
Commercial Distribution Discontinuation | 2023-02-01 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MediMeter |
Version Model Number | MM30 _O2 DS _ 9/16UNF G |
Catalog Number | 0730106US |
Company DUNS | 819753190 |
Company Name | GCE, s.r.o. |
Device Count | 1 |
DM Exempt | false |
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 | true |
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 | false |