Primary Device ID | ENOU20260 |
NIH Device Record Key | fc6c1fe8-2acf-474d-bdce-47cfad40682f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MD 11 |
Version Model Number | 2026 |
Company DUNS | 480610476 |
Company Name | Nouvag AG |
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 | true |
OTC Over-The-Counter | false |
Phone | +41718466600 |
info@nouvag.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | ENOU20260 [Primary] |
DZI | Drill, Bone, Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[ENOU20260]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-13 |
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