Primary Device ID | 76401109877044 |
NIH Device Record Key | 63f399b1-24a4-461f-9227-922371e6e437 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Low Profile Peripheral |
Version Model Number | 616.460.7070-A |
Catalog Number | 616.460.7070-A |
Company DUNS | 097736867 |
Company Name | PFM MEDICAL INCORPORATED |
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 | 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 |
Phone | 7607588749 |
customerservice@pfmmedicalusa. | |
Phone | 7607588749 |
customerservice@pfmmedicalusa. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 76401109877044 [Primary] |
LJT | Port & Catheter, Implanted, Subcutaneous, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-23 |
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