Primary Device ID | G0561067301 |
NIH Device Record Key | 2d47ee02-83d8-4dad-b959-aaf521ad7860 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | vW Select Kit (Ristocetin Cofactor) |
Version Model Number | 106730 |
Catalog Number | 106730 |
Company DUNS | 051392959 |
Company Name | Bio/Data Corporation |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | G0561067301 [Primary] |
GGP | Test, Qualitative And Quantitative Factor Deficiency |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-31 |
Device Publish Date | 2022-03-23 |
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