Primary Device ID | D757X80496B1 |
NIH Device Record Key | 7b8259ec-1eb8-473b-b398-dce176b6bb7d |
Commercial Distribution Discontinuation | 2023-01-17 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Disposable Mixing Well 48/PK-Double Well |
Version Model Number | X-80496B |
Catalog Number | X-80496B |
Company DUNS | 053529939 |
Company Name | BISCO INC. |
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 | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com | |
Phone | +1(847)534-6000 |
sales@bisco.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D757X80496B1 [Primary] |
KXR | APPLICATOR, RESIN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-05-04 |
Device Publish Date | 2018-11-06 |
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