Primary Device ID | 00081317020028 |
NIH Device Record Key | 3151bd97-a4f1-4872-a64e-a039e8520a9a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Accelerator II, Aspirator (110V) |
Version Model Number | ASP II |
Catalog Number | ASP II |
Company DUNS | 167450993 |
Company Name | MENTOR TEXAS L.P. |
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 | false |
Serial Number | true |
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 | +1(800)235-5731 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00081317020028 [Primary] |
MUU | System, suction, lipoplasty |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-23 |
Device Publish Date | 2016-09-14 |
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