Primary Device ID | 04260632792308 |
NIH Device Record Key | 8b3fb72a-d1e0-43e1-8885-980ee9fdc4b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liposat Pro plus |
Version Model Number | 00003974 |
Company DUNS | 320405061 |
Company Name | Möller Medical GmbH |
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 | true |
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 | 04260632792308 [Primary] |
MUU | System, Suction, Lipoplasty |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-29 |
Device Publish Date | 2020-01-21 |
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