Primary Device ID | 50886333622394 |
NIH Device Record Key | f5fd6437-bcad-4f03-a3fd-df17163342f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COMP PRLINE FM 120CM CLR |
Version Model Number | 682239 |
Catalog Number | 682239 |
Company DUNS | 595138793 |
Company Name | ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com | |
Phone | 1.800.927.4669 |
Customer.Service@argonmedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886333622399 [Primary] |
GS1 | 50886333622394 [Package] Contains: 00886333622399 Package: Tyvek Bag [125 Units] In Commercial Distribution |
DRS | Transducer, Blood-Pressure, Extravascular |
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 | 2016-09-30 |
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