Primary Device ID | 00817688020332 |
NIH Device Record Key | 968e114c-bbd3-4f97-a8e3-5f59bf913499 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultra Vac |
Version Model Number | 3110-10 |
Catalog Number | ICM-000-0484 |
Company DUNS | 616182895 |
Company Name | I.C. MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817688020325 [Primary] |
GS1 | 00817688020332 [Package] Contains: 00817688020325 Package: [20 Units] In Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-04-08 |
Device Publish Date | 2016-09-24 |
00817688020356 | 3110-10EC |
00817688020332 | 3110-10 |
00817688020318 | 2110-10EC |
00817688020295 | 2110-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ULTRA VAC 87124759 5325102 Live/Registered |
GHAZARIAN WELDING INC. 2016-08-02 |