Primary Device ID | 00840828153973 |
NIH Device Record Key | a44070df-d54c-4158-a94b-0214ba74bd12 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RLW,6LD,SNAP,ML,MX,AHA |
Version Model Number | RLW-06AD-MXAS-0000 |
Catalog Number | 20246 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |
Phone | 1-800-235-7500 |
mwinter@curbell.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840828153973 [Primary] |
DSA | Cable, Transducer And Electrode, Patient, (Including Connector) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-10-20 |
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