Primary Device ID | 10878799004908 |
NIH Device Record Key | 67284f3d-b795-4307-b2f2-9ab1383b0691 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgistar |
Version Model Number | 125008 |
Company DUNS | 808865125 |
Company Name | SURGISTAR, 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com | |
Phone | 7605982480 |
customerservice@surgistar.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00878799004901 [Primary] |
GS1 | 10878799004908 [Package] Contains: 00878799004901 Package: [10 Units] In Commercial Distribution |
HMX | Cannula, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-04 |
Device Publish Date | 2021-02-24 |