Primary Device ID | EIBAM90063300 |
NIH Device Record Key | c1c398c8-ff3e-4588-9684-b1ade425d2da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Detector Holder |
Version Model Number | M9006330 |
Catalog Number | DA07-800 |
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 | false |
Manufacturing Date | false |
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 | +1 901 386-2242 |
USService@iba-group.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | EIBAM90063300 [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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-09 |
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