| Primary Device ID | 00850040139402 |
| NIH Device Record Key | d79f71cc-93c0-45f9-9a0b-e460be069e41 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Site Prep Locator - Row Series |
| Version Model Number | SR07-6010 |
| Company DUNS | 004095409 |
| Company Name | SURGENTEC, LLC |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Expiration Date | true |
| 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 | 00850040139402 [Primary] |
| PDQ | Neurosurgical Nerve Locator |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
[00850040139402]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-13 |
| Device Publish Date | 2025-01-03 |