Primary Device ID | 00852621004734 |
NIH Device Record Key | 36101610-053a-46a3-bcf8-6ea61e7d8a49 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Greyhound |
Version Model Number | N10157NS |
Catalog Number | N10157NS |
Company DUNS | 121464288 |
Company Name | VITALITEC INTERNATIONAL, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 5087476033 |
eknupp@aol.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852621004734 [Primary] |
GS1 | 10852621004731 [Package] Package: Case [100 Units] In Commercial Distribution |
DXC | Clamp, Vascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00852621004734]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-26 |
00852621004734 | Vascular Clamp |
00852621004048 | Vascular Clamp |