| Primary Device ID | 88806182210392 |
| NIH Device Record Key | 49ae77e9-b6d1-45d3-98a6-796d0f15493a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Laport |
| Version Model Number | N21-0575 |
| Catalog Number | N21-0575 |
| Company DUNS | 689850476 |
| Company Name | Sejong Medical Co., Ltd |
| 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 | false |
| 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 |
| Phone | +821075249166 |
| global2@sejongmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08806182210396 [Primary] |
| GS1 | 18806182210393 [Package] Contains: 08806182210396 Package: INBOX [10 Units] In Commercial Distribution |
| GS1 | 88806182210392 [Package] Contains: 18806182210393 Package: CARTON [8 Units] In Commercial Distribution |
| GCJ | Laparoscope, General & Plastic Surgery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-09 |
| Device Publish Date | 2018-04-05 |
| 88806182210873 | N20-0510 |
| 88806182210583 | N23-1210 |
| 88806182210514 | N23-0575 |
| 08806182210433 | N21-1110 |
| 88806182210392 | N21-0575 |
| 88806182210378 | N21-0510 |
| 88806182210330 | N22-0510 |