Primary Device ID | 04260277174460 |
NIH Device Record Key | 133392ce-2fd4-428b-9062-91965a3d95cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Injection cannula 3 |
Version Model Number | 10001184 |
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 | 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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04260277174460 [Primary] |
MUU | System, Suction, Lipoplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-23 |
Device Publish Date | 2016-09-24 |
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