Primary Device ID | 00850645007175 |
NIH Device Record Key | 8d2e9328-9f0e-420d-b62d-5e6f4dd2e68d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AOS Implant Tube, Intralumenal |
Version Model Number | TII0005-001 |
Company DUNS | 060398989 |
Company Name | ALPHA-OMEGA SERVICES, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850645007175 [Primary] |
JAQ | System, Applicator, Radionuclide, Remote-Controlled |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
[00850645007175]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-10-05 |
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