Primary Device ID | 00817051020815 |
NIH Device Record Key | 65342ee8-2988-47ad-9746-7d0b1d015045 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NoCord VPS |
Version Model Number | 310285 |
Company DUNS | 053707303 |
Company Name | CENTRIX, 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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 00817051020815 [Primary] |
MVL | Cord, Retraction |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-23 |
00817051020815 | NoCord VPS System Refill impression material |
00817051020808 | NoCord VPS Retraction Wash impression material, 10 pk |
00817051020792 | NoCord VPS MegaBody impression material, 10 pk |
00817051020785 | NoCord VPS Retraction Wash impression material, 2 pk |
00817051020778 | NoCord VPS MegaBody impression material, 2 pk |
00817051020761 | NoCord VPS impression material Introduction Kit |