Primary Device ID | 10386040004107 |
NIH Device Record Key | ac9e327a-c613-4b13-9581-f11db38df14f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GC CARTRIDGE DISPENSER II |
Version Model Number | 152101 |
Catalog Number | 152101 |
Company DUNS | 005473608 |
Company Name | Gc America 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 | false |
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 |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com | |
Phone | +1(708)597-0900 |
customerservice@gcamerica.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10386040004107 [Primary] |
ELW | MATERIAL, IMPRESSION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-15 |
Device Publish Date | 2022-07-07 |
10386040006156 | GC CARTRIDGE DISPENSER II Plunger Conversion Kit, 75mL |
10386040006149 | GC CARTRIDGE DISPENSER II Plunger, 48mL |
10386040006132 | GC CARTRIDGE DISPENSER II 75mL |
10386040004107 | GC CARTRIDGE DISPENSER II 48mL |