Primary Device ID | 10801741012461 |
NIH Device Record Key | bd588121-1780-49ed-bd87-1042f31dee1e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Catheter Repair Kit |
Version Model Number | 5581000 |
Catalog Number | 5581000 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741012464 [Primary] |
GS1 | 10801741012461 [Package] Contains: 00801741012464 Package: CA [5 Units] In Commercial Distribution |
GS1 | 20801741012468 [Package] Package: BX [60 Units] In Commercial Distribution |
MSD | Catheter, hemodialysis, implanted |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-05-06 |
20801741045107 | Catheter Repair Kit |
10801741045087 | Catheter Repair Kit with Replacement Connector |
10801741012461 | DUET CATHETER REPAIR KIT |