| Primary Device ID | 30705036011914 |
| NIH Device Record Key | 033c465c-0efe-4801-a09a-0b3a5b89a3bf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FLEXIPATH |
| Version Model Number | FP015 |
| Catalog Number | FP015 |
| Company DUNS | 044606982 |
| Company Name | ETHICON ENDO-SURGERY, LLC |
| Device Count | 6 |
| 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 | false |
| 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 | 10705036011910 [Unit of Use] |
| GS1 | 20705036011917 [Primary] |
| GS1 | 30705036011914 [Package] Contains: 20705036011917 Package: CASE [36 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 | 2019-07-08 |
| Device Publish Date | 2016-07-15 |
| 30705036011921 | Flexipath Flexible Surgical Trocars |
| 30705036011914 | Flexipath Flexible Surgical Trocars |
| 30705036011907 | Flexipath Flexible Surgical Trocars |
| 30705036001991 | Flexipath Flexible Surgical Trocar Paks |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FLEXIPATH 98648562 not registered Live/Pending |
Shenzhen Aiper Intelligent Co., Ltd. 2024-07-15 |
![]() FLEXIPATH 74560195 1908311 Live/Registered |
JOHNSON & JOHNSON 1994-08-11 |