Primary Device ID | 18148440000255 |
NIH Device Record Key | 685b40d5-c802-46a5-902b-88aaa6d2b6aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Infinity Enteral Spike Right Administration Set with Enfit Connector |
Version Model Number | INF0020-A |
Company DUNS | 612746933 |
Company Name | ZEVEX 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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com | |
Phone | 800-970-2337 |
medcustomerservice@moog.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18148440000255 [Primary] |
GS1 | 38148440000259 [Package] Package: [30 Units] In Commercial Distribution |
PIF | Gastrointestinal Tubes With Enteral Specific Connectors |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-10-20 |
18148440000255 | INF0020-A |
30814844000253 | INF0020-A |