Primary Device ID | 10801741182911 |
NIH Device Record Key | 926e2136-a718-4637-b659-1c74250967dd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PowerLoc MAX |
Version Model Number | CPA00057 |
Catalog Number | CPA00057 |
Company DUNS | 044611812 |
Company Name | Bard Access Systems, Inc. |
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 | true |
Device Combination Product | true |
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 |
Phone | +1(800)545-0890 |
medical.services@crbard.com | |
Phone | +1(800)545-0890 |
medical.services@crbard.com |
Length | 0.75 Inch |
Length | 0.75 Inch |
Length | 0.75 Inch |
Length | 0.75 Inch |
Storage Environment Temperature | Between 20 Degrees Celsius and 25 Degrees Celsius |
Storage Environment Temperature | Between 20 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00801741182914 [Primary] |
GS1 | 10801741182911 [Package] Contains: 00801741182914 Package: CA [5 Units] In Commercial Distribution |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-11-13 |
10801741183017 | Port Access Kit |
10801741183000 | Port Access Kit |
10801741182997 | Port Access Kit |
10801741182911 | Port Access Kit |
10801741182904 | Port Access Kit |
20801741235256 | Port Access Kit |
10801741235242 | Port Access Kit |
10801741235235 | Port Access Kit |