Primary Device ID | 05902729750455 |
NIH Device Record Key | bae762c6-3670-48c4-8d6b-079fa18411b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CT Preparation |
Version Model Number | 2017-1 |
Company DUNS | 305500094 |
Company Name | 3shape Medical A/S |
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 | true |
Serial Number | false |
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 | +4570272620 |
support@3shape.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05902729750455 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-02 |
Device Publish Date | 2018-02-28 |
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