Primary Device ID | 30023185474764 |
NIH Device Record Key | 6a8b1777-8ccd-452d-8d4c-04094654b1ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PREFERRED PLUS PHARMACY ++++ & Design |
Version Model Number | 4437448 |
Catalog Number | 4437448 |
Company DUNS | 012574513 |
Company Name | KINRAY, 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 | false |
Lot Batch | true |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00023185474763 [Primary] |
GS1 | 30023185474764 [Package] Contains: 00023185474763 Package: BOX [6 Units] In Commercial Distribution |
GS1 | 50023185474768 [Package] Package: CASE [6 Units] In Commercial Distribution |
OHY | Pill crusher/cutter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-29 |
Device Publish Date | 2019-10-21 |