Primary Device ID | 00841365117503 |
NIH Device Record Key | 9436bdd3-7274-4b6e-b4f8-3caf30cab8c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Best Medical International |
Version Model Number | 501-2 |
Company DUNS | 086352655 |
Company Name | BEST MEDICAL INTERNATIONAL, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00841365117503 [Primary] |
KXK | Source, Brachytherapy, Radionuclide |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
[00841365117503]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-17 |
Device Publish Date | 2019-10-09 |