Primary Device ID | 09120074396753 |
NIH Device Record Key | af31568f-74e9-467f-be55-7b9230faf96c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U14 Indexing Bar MR Glasfaser for Varian |
Version Model Number | P10107-675 |
Company DUNS | 300005408 |
Company Name | IT-V Medizintechnik 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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09120074396753 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-19 |
Device Publish Date | 2024-03-11 |
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