| Primary Device ID | 00813110024237 |
| NIH Device Record Key | 8c4350ed-058d-45af-8bac-47d6bc99e7be |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Guide Pin |
| Version Model Number | 260-101-180 |
| Catalog Number | 260-101-180 |
| Company DUNS | 945015758 |
| Company Name | BICON, LLC |
| Device Count | 4 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | 617-524-4443 |
| support@bicon.com | |
| Phone | 617-524-4443 |
| support@bicon.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813110024237 [Primary] |
| GS1 | 10813110024234 [Unit of Use] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00813110024237]
Moist Heat or Steam Sterilization
[00813110024237]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-03-25 |
| Device Publish Date | 2016-05-06 |
| 00813110024251 | 2.5mm Standard Guide Pin |
| 00813110024244 | 3.0mm Standard Guide Pin |
| 00813110024237 | 2.0mm Standard Guide Pin |
| 10813110024234 | 2.5mm Guide Pin - Tall Post (4) |