Primary Device ID | EIBADS50002XLT0 |
NIH Device Record Key | 522c1d8a-69bc-401c-9c5f-1df6b36aa320 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stealth Chamber |
Version Model Number | DS50-002-XL-T |
Company DUNS | 332599307 |
Company Name | IBA Dosimetry 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 | 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 |
Phone | +49912860738 |
service@iba-group.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EIBADS50002XLT0 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-09 |
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