Primary Device ID | 00817688021841 |
NIH Device Record Key | e807aaeb-b845-4a6c-b0d6-da620e240b29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mega Vac |
Version Model Number | 2100 |
Catalog Number | ICM-360-0002 |
Company DUNS | 616182895 |
Company Name | I.C. MEDICAL, INC. |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817688021841 [Primary] |
FYD | Apparatus, Exhaust, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-04-08 |
Device Publish Date | 2016-09-24 |
00817688022367 | ICM-360-0002 |
00817688021841 | 2100 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MEGA VAC 88485926 not registered Live/Pending |
Duct Doctor Ltd. 2019-06-24 |
![]() MEGA VAC 86580158 not registered Dead/Abandoned |
Duct Doctor Ltd. 2015-03-29 |
![]() MEGA VAC 75300129 not registered Dead/Abandoned |
Duct Cleaners' Supply/A Division of Duct Doctor, Ltd. 1997-05-29 |