Primary Device ID | 30705031202744 |
NIH Device Record Key | 8a1c2f32-9950-49cf-ae61-304f39e2dff2 |
Commercial Distribution Discontinuation | 2019-05-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ETHICON SECURESTRAP |
Version Model Number | OPENSTRAP20 |
Catalog Number | OPENSTRAP20 |
Company DUNS | 079402290 |
Company Name | ETHICON, LLC |
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 | 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 |
Phone | +1(877)384-4266 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705031202757 [Primary] |
GS1 | 30705031202744 [Package] Contains: 10705031202757 Package: BOX [6 Units] Discontinued: 2019-05-16 Not in Commercial Distribution |
GDW | STAPLE, IMPLANTABLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-16 |
Device Publish Date | 2015-09-23 |
30705031202744 | Absorbable Strap Fixation Device |
30705031231058 | Absorbable Strap Fixation Device |
30705031132973 | Absorbable Strap Fixation Device |
30705031132980 | Absorbable Strap Fixation Device |
10705031470552 | ETHICON SECURESTRAP ABSORBABLE FIXATION DEVICE |
10705031470569 | ETHICON SECURESTRAP ABSORBABLE FIXATION DEVICE |
10705031470576 | ETHICON SECURESTRAP ABSORBABLE FIXATION DEVICE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ETHICON SECURESTRAP 77843408 4150544 Live/Registered |
JOHNSON & JOHNSON 2009-10-07 |