Primary Device ID | 00841365119156 |
NIH Device Record Key | 064b9510-3736-46b8-addd-f731f4a5f042 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Best Medical International |
Version Model Number | 296-25.3 |
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 | 00841365119156 [Primary] |
IWJ | System, Applicator, Radionuclide, Manual |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
[00841365119156]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-05 |
Device Publish Date | 2021-07-28 |