Primary Device ID | 07908823600137 |
NIH Device Record Key | 566b4a8b-6cef-45f7-937a-edcab73df2b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biotecno |
Version Model Number | BT-1200/280l |
Company DUNS | 760374974 |
Company Name | BIOTECNO INDUSTRIA E COMERCIO LTDA |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07908823600137 [Primary] |
KSE | Refrigerator, Freezer, Blood Storage |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-14 |
Device Publish Date | 2024-08-06 |
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