Primary Device ID | 20884450320918 |
NIH Device Record Key | d50cea5e-c4e7-4410-aa88-bf6271442cea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Critikit™ |
Version Model Number | 10884450320911 |
Catalog Number | 680002/A |
Company DUNS | 595138793 |
Company Name | ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. |
Device Count | 5 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450320914 [Unit of Use] |
GS1 | 10884450320911 [Primary] |
GS1 | 20884450320918 [Package] Contains: 10884450320911 Package: [10 Units] In Commercial Distribution |
KRB | PROBE, THERMODILUTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-12-13 |
Device Publish Date | 2018-01-30 |
20884450557109 | 10884450557102 |
20884450320932 | 10884450320935 |
20884450320918 | 10884450320911 |
20884450320901 | 10884450320904 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CRITIKIT 73559830 1427350 Live/Registered |
GOULD INC. 1985-09-23 |