Primary Device ID | 08059307490702 |
NIH Device Record Key | dd20344f-f9df-4ad3-8766-140b1e91f4da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RTM 90 HS |
Version Model Number | 0.6/1.3 |
Company DUNS | 430263475 |
Company Name | I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE SPA |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08059307490702 [Primary] |
ITY | Assembly, Tube Housing, X-Ray, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-02 |
Device Publish Date | 2020-08-25 |
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