Primary Device ID | 05708265004959 |
NIH Device Record Key | 98450ebb-50ab-4014-bb99-bba343e5c100 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Meniett™ Power Cord, Continental Europe |
Version Model Number | MT-CAB-EU |
Catalog Number | MT-CAB-EU |
Company DUNS | 305088619 |
Company Name | Lina Medical ApS |
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 | 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 |
Phone | +48612222140 |
info.poland@lina-medical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05708265004959 [Primary] |
ETY | Tester, Auditory Impedance |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-11-16 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MENIETT 78100193 2882865 Live/Registered |
LINA MEDICAL APS 2001-12-28 |
MENIETT 76318095 not registered Dead/Abandoned |
Pascal Medical AB 2001-09-27 |