Primary Device ID | 10848340009645 |
NIH Device Record Key | 37c7f005-3b47-4021-ad96-e1e677e2c6d7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UNBRANDED |
Version Model Number | CC211NS |
Company DUNS | 130785884 |
Company Name | ADVANCE MEDICAL DESIGNS, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00848340009648 [Primary] |
GS1 | 10848340009645 [Package] Contains: 00848340009648 Package: [500 Units] In Commercial Distribution |
JAA | System, x-ray, fluoroscopic, image-intensified |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10848340009645]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-27 |