Primary Device ID | 00857235006037 |
NIH Device Record Key | 8afd1392-07a7-450a-9e5c-415b8ee74d8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Varian Halcyon |
Version Model Number | 3.0 |
Company DUNS | 009120817 |
Company Name | VARIAN MEDICAL SYSTEMS, INC. |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857235006037 [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 | 2020-02-24 |
Device Publish Date | 2020-02-14 |
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