Primary Device ID | 00609960000893 |
NIH Device Record Key | 5a7f1acc-551c-4f88-ae14-8bcaf94b78b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Geiger TCU Reusable Electrode |
Version Model Number | 201-D |
Catalog Number | 201-D |
Company DUNS | 021628771 |
Company Name | DERMATOLOGIC LAB AND SUPPLY, INC. |
Device Count | 1 |
DM Exempt | true |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00609960000893 [Primary] |
HQO | Unit, Cautery, Thermal, Ac-Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00609960000893]
Moist Heat or Steam Sterilization
[00609960000893]
Moist Heat or Steam Sterilization
[00609960000893]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-08-29 |
Device Publish Date | 2018-07-10 |
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