Primary Device ID | B154R39101420030 |
NIH Device Record Key | 6855e9cd-4ba6-451c-91ab-e8f4fa0f7ef6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cannula 3mm SS, Non-Sterile |
Version Model Number | 3mm SS |
Catalog Number | 3910142.003 |
Company DUNS | 556957871 |
Company Name | WATERS MEDICAL SYSTEMS, LLC |
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 | false |
Phone | 507-288-7777 |
info@wtrs.com | |
Phone | 507-288-7777 |
info@wtrs.com |
Lumen/Inner Diameter | 3 Millimeter |
Lumen/Inner Diameter | 3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B154R39101420030 [Primary] |
KDN | System, Perfusion, Kidney |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B154R39101420030]
Moist Heat or Steam Sterilization
[B154R39101420030]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-03-20 |
Device Publish Date | 2018-05-02 |
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