Primary Device ID | 10840067101381 |
NIH Device Record Key | 22a835e4-9ddb-4dc2-94ed-75f8bb615c10 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cadwell Bar Electrodes |
Version Model Number | 302287-000 |
Company DUNS | 098554157 |
Company Name | CADWELL INDUSTRIES, INC. |
Device Count | 200 |
DM Exempt | true |
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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(509)735-6481 |
applications@cadwell.com |
Length | 2.33 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840067101384 [Primary] |
GS1 | 10840067101381 [Package] Contains: 00840067101384 Package: Case [60 Units] In Commercial Distribution |
GS1 | 20840067101388 [Unit of Use] |
GXY | ELECTRODE, CUTANEOUS |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-22 |
Device Publish Date | 2016-09-05 |
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