Lapra-TY KA200
GUDID 10705036012641
Lapra-TY Suture Clip Applier 33cm Shaft Length -11mm Diameter
ETHICON ENDO-SURGERY, LLC
Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier Open-surgery ligation clip applier| Primary Device ID | 10705036012641 |
| NIH Device Record Key | ae099f4b-baee-4989-aaa2-9423ee2b6379 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lapra-TY |
| Version Model Number | KA200 |
| Catalog Number | KA200 |
| Company DUNS | 044606982 |
| Company Name | ETHICON ENDO-SURGERY, LLC |
| Device Count | 1 |
| 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 | false |
| 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 |
Customer Support Contacts
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10705036012641 [Direct Marking] |
| GS1 | 20705036012648 [Primary] |
| GS1 | 30705036012645 [Package] Contains: 20705036012648 Package: CASE [3 Units] In Commercial Distribution |
| GS1 | 40705036012642 [Package] Contains: 20705036012648 Package: CASE [10 Units] In Commercial Distribution |
FDA Product Code
| GDO | Applier, surgical, clip |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
[10705036012641]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-28 |
| Device Publish Date | 2016-07-15 |
Devices Manufactured by ETHICON ENDO-SURGERY, LLC
| 20705036027857 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 100mm BLUE |
| 30705036027861 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 100mm GREEN |
| 20705036027871 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 60mm BLUE |
| 40705036027882 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 60mm GREEN |
| 30705036027892 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 80mm BLUE |
| 30705036027908 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter Reload 80mm GREEN |
| 30705036030878 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter 60mm |
| 30705036030885 - Echelon Linear Cutter | 2024-04-23 Echelon Linear Cutter 80mm |
Trademark Results [Lapra-TY]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LAPRA-TY 74458470 1887046 Live/Registered |
JOHNSON & JOHNSON 1993-11-15 |
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