Primary Device ID | M328RV000106 |
NIH Device Record Key | 6381a71f-8c17-4848-9470-c9bab15ceb62 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Revolve Advanced Adipose System |
Version Model Number | RV0001 |
Company DUNS | 157224205 |
Company Name | LIFECELL CORPORATION |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-367-5737 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00818410012267 [Secondary] |
HIBCC | M328RV000106 [Primary] |
HIBCC | M328RV000207 [Package] Package: Case [2 Units] In Commercial Distribution |
HIBCC | M328RV000409 [Package] Package: Case [4 Units] In Commercial Distribution |
MUU | System, Suction, Lipoplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2016-09-24 |
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