| Primary Device ID | 00609960001067 |
| NIH Device Record Key | a9ad79c5-44e3-4dcf-a00a-2b59b2a0f6e2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Geiger Reusable TCU Electrodes |
| Version Model Number | 203-D |
| Catalog Number | 203-D |
| Company DUNS | 021628771 |
| Company Name | DERMATOLOGIC LAB AND SUPPLY, INC. |
| Device Count | 1 |
| 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 | 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 | 00609960001067 [Primary] |
| HQO | Unit, Cautery, Thermal, Ac-Powered |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00609960001067]
Moist Heat or Steam Sterilization
[00609960001067]
Moist Heat or Steam Sterilization
[00609960001067]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-08-10 |
| Device Publish Date | 2018-07-10 |
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