| Primary Device ID | 00810125994920 |
| NIH Device Record Key | dbaa7737-2590-45db-b8ef-45d56c73ab43 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET PICK-UP GUIDE PIN |
| Version Model Number | ETPGPM100C |
| Company DUNS | 796083090 |
| Company Name | HIOSSEN, INC. |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810125994920 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-15 |
| Device Publish Date | 2024-07-06 |
| 00814913025728 | ETFPG10SL |
| 00814913025711 | ETFPG05SL |
| 00814913025704 | ETFPG05S |
| 00814913025698 | ETFPG00SL |
| 00814913025681 | ETFPG00S |
| 00814913025674 | ETFPG10ML |
| 00814913025667 | ETFPG05ML |
| 00814913025650 | ETFPG05M |
| 00814913025643 | ETFPG00ML |
| 00814913025636 | ETFPG00M |
| 00810125995019 | ETPGPR200LC |
| 00810125995002 | ETPGPR150LC |
| 00810125994999 | ETPGPR150C |
| 00810125994982 | ETPGPR100LC |
| 00810125994975 | ETPGPR100C |
| 00810125994968 | ETPGPM200LC |
| 00810125994951 | ETPGPM150LC |
| 00810125994944 | ETPGPM150C |
| 00810125994937 | ETPGPM100LC |
| 00810125994920 | ETPGPM100C |