Primary Device ID | H97113515026 |
NIH Device Record Key | 8f4b8943-b69d-4ed8-beab-fd4fc04528a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CaviWipes1 XL |
Version Model Number | 13-5150 |
Company DUNS | 145963778 |
Company Name | METREX RESEARCH, LLC |
Device Count | 65 |
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 | 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 | false |
OTC Over-The-Counter | true |
Phone | +18008411428 |
customercare@kavokerrgroup.com | |
Phone | +18008411428 |
customercare@kavokerrgroup.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00615375004999 [Primary] |
GS1 | 00615375007716 [Unit of Use] |
HIBCC | H97113515026 [Secondary] |
LRJ | Disinfectant, medical devices |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-05-23 |
Device Publish Date | 2016-08-31 |
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