| Primary Device ID | 00609960000312 |
| NIH Device Record Key | 54115dfd-6775-491d-8809-d6f9ca1068b1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Segal Electrode |
| Version Model Number | SEGAL |
| Catalog Number | SEGAL |
| Company DUNS | 021628771 |
| Company Name | DERMATOLOGIC LAB AND SUPPLY, INC. |
| Device Count | 1 |
| 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 | false |
| Lot Batch | false |
| 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 | 00609960000312 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00609960000312]
Moist Heat or Steam Sterilization
[00609960000312]
Moist Heat or Steam Sterilization
[00609960000312]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-08-29 |
| Device Publish Date | 2016-05-19 |
| 00609960000404 | SEGAL ELECTRODE, NEEDLE,2 1/2inLENGTH, 3/32in |
| 00609960000398 | SEGAL ELECTRODE, NEEDLE, 4 3/4inLENGTH, 3/32in |
| 00609960000381 | SEGAL ELECTRODE, LOOP, REUSABLE, 3/32in |
| 00609960000350 | SEGAL ELECTRDE,7/32inBALL4 3/4inLONG,STRAIGHT |
| 00609960000343 | SEGAL ELECTRDE,5/32inBALL1 3/4inLONG,STRAIGHT |
| 00609960000336 | SEGAL ELECTRODE, BALL, ANGLED, 3/32in |
| 00609960000312 | ELECTRODE, SEGAL 3/32in POLISHED, ANGLED This device is subject to direct marking, but excepted |
| 00609960001289 | SEGAL ELECTRODE, GENERAL PURPOSE, 3/32in EACH |