Primary Device ID | 00852244007402 |
NIH Device Record Key | d02589e6-fd3a-45e6-a68c-4b085d9e2692 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KENTRON CAPNOGRAPHY |
Version Model Number | 587500 |
Catalog Number | 587500 |
Company DUNS | 618825723 |
Company Name | KENTRON HEALTHCARE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com | |
Phone | 615-384-0573 |
kentron@kentronmedical.com |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Length | 7 Feet |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852244007402 [Package] Contains: 10852244007409 Package: CASE [50 Units] In Commercial Distribution |
GS1 | 10852244007409 [Primary] |
CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-03-22 |
Device Publish Date | 2016-09-16 |
00852244007464 | OXYGEN NASAL CANNULA INFANT 7FT TUBE, W/CO2, SAMPLING LINE (MALE LUER) |
10852244007454 | OXYGEN NASAL CANNULA CHILD 7FT TUBE, W/CO2, SAMPLING LINE (MALE LUER) |
00852244007440 | OXYGEN NASAL CANNULA ADULT 7FT TUBE, W/CO2, SAMPLING LINE (MALE LUER) |
00852244007433 | NASAL CANNULA INFANT 7FT TUBE, W/CO2, SAMPLING LINE (FEMALE LUER) |
00852244007426 | NASAL CANNULA CHILD 7FT TUBE, W/CO2, SAMPLING LINE (FEMALE LUER) |
00852244007419 | NASAL CANNULA ADULT 7FT TUBE, W/CO2, SAMPLING LINE (FEMALE LUER) |
00852244007402 | OXYGEN NASAL CANNULA INFANT 7FT TUBE, W/CO2 SAMPLING LINE (MALE LUER) |
00852244007396 | OXYGEN NASAL CANNULA CHILD 7FT TUBE, W/CO2 SAMPLING LINE (MALE LUER) |
00852244007389 | OXYGEN NASAL CANNULA ADULT 7FT TUBE, W/CO2 SAMPLING LINE (MALE LUER) |