Primary Device ID | G6192110411 |
NIH Device Record Key | 3fa17633-bc93-4c3f-9bf9-543fe676a840 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JK-RUSA |
Version Model Number | 400W R7s |
Catalog Number | 21104-1 |
Company DUNS | 039280558 |
Company Name | JW NORTH AMERICA, 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
---|---|
HIBCC | B5331181200 [Previous] |
HIBCC | G6192110410 [Primary] |
HIBCC | G6192110411 [Package] Contains: G6192110410 Package: carton box [25 Units] In Commercial Distribution |
HIBCC | G6192110412 [Package] Contains: G6192110410 Package: carton box [50 Units] In Commercial Distribution |
LEJ | Booth, Sun Tan |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-09 |
Device Publish Date | 2024-08-01 |
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