Primary Device ID | 00862393000117 |
NIH Device Record Key | 6f17a211-ab0d-4f62-b2f4-45ca2da75ad8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Minerva Disposable Handpieces |
Version Model Number | MIN3PAK |
Catalog Number | MIN3PAK |
Company DUNS | 829616478 |
Company Name | Minerva Surgical, Inc. |
Device Count | 3 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00862393000117 [Primary] |
GS1 | 86239300011703 [Unit of Use] |
MNB | Device, Thermal Ablation, Endometrial |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2017-06-27 |
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