Primary Device ID | 30705036011921 |
NIH Device Record Key | 488b3c72-8a7b-4389-b3fb-4437888f0daf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FLEXIPATH |
Version Model Number | FP020 |
Catalog Number | FP020 |
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 | 10705036011927 [Unit of Use] |
GS1 | 20705036011924 [Primary] |
GS1 | 30705036011921 [Package] Contains: 20705036011924 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 |