Primary Device ID | 10865382000218 |
NIH Device Record Key | 80ca0933-4708-47f2-b518-0667844c7fce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SecurAcath |
Version Model Number | 4F |
Catalog Number | 400140 |
Company DUNS | 555472310 |
Company Name | INTERRAD MEDICAL, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Catheter Gauge | 4 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00865382000211 [Primary] |
GS1 | 10865382000218 [Package] Contains: 00865382000211 Package: Shelf Box [10 Units] In Commercial Distribution |
OKC | Implanted Subcutaneous Securement Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2016-09-15 |
10865382000256 | 8F |
10865382000249 | 7F |
10865382000232 | 6F |
10865382000225 | 5F |
10865382000218 | 4F |
10865382000201 | 3F |
00865382000297 | 10F |
00865382000280 | 12F |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SECURACATH 85591187 4348913 Live/Registered |
Interrad Medical, Inc. 2012-04-06 |
SECURACATH 78703147 4071317 Live/Registered |
Interrad Medical, Inc. 2005-08-30 |
SECURACATH 74353255 1813589 Dead/Cancelled |
HDC, Inc. 1993-01-28 |