Primary Device ID | 00852621004048 |
NIH Device Record Key | 18c56f0d-24cd-42c2-83d1-d0702f4de972 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Greyhound |
Version Model Number | N10157 |
Catalog Number | N10157 |
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 | true |
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 | 00852621004048 [Primary] |
GS1 | 10852621004045 [Package] Package: Case [15 Units] In Commercial Distribution |
DXC | Clamp, Vascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
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 |