Home GUDID 05700699056894 TC contact liquid
Primary DI 05700699056894
Brand TC contact liquid
Company Radiometer Medical ApS
Model 905-689
Catalog number 905-689
Device description Contact Liquid 4 x 20 mL.
Published 2016-09-01
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false
Product Codes# Code, Name table Code Name DQA Oximeter KLK Monitor, oxygen, cutaneous, for infant not under gas anesthesia LKD MONITOR, CARBON-DIOXIDE, CUTANEOUS LPP Monitor, oxygen, cutaneous, for uses other than for infant not under gas anesthesia
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQA Oximeter Cardiovascular 2 KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia Anesthesiology 2 LKD Monitor, Carbon-Dioxide, Cutaneous Anesthesiology 2 LPP Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia Anesthesiology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 05700699056894 Primary GS1 0 55700699056899 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 05700699056894 05700699056894 5700699056894 55700699056899 55700699056899
GMDN Terms# Term, Definition table Term Definition Transcutaneous blood gas monitor sensor A device intended to be used with a transcutaneous blood gas monitor to measure a patient's blood partial pressure of oxygen (pO2), blood partial pressure of carbon dioxide (pCO2), and/or blood oxygen saturation transcutaneously (through the skin). Gases diffuse through the skin and into this sensor at the skin surface, where it transmits electrical signals to the parent device for analysis. This is a reusable device.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 0 0
Regulatory Flags# DUNS number 308667539 Device count 4 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 05700693930978 ABL90 FLEX 393-097 393-097 2026-07-09 05700693930985 ABL90 FLEX PLUS 393-098 393-098 2026-07-09 05700699446572 SP90 944-657 944-657 2026-07-09 05700699447579 SP90 944-757 944-757 2026-07-09 05700699461056 SC90 946-105 946-105 2026-07-09 05700699461087 SC90 946-108 946-108 2026-07-09 05700699461094 SC90 946-109 946-109 2026-07-09 05700699461100 SC90 946-110 946-110 2026-07-09 05700699461131 SC90 946-113 946-113 2026-07-09 05700699461605 SC90 946-160 946-160 2026-07-09 05700699428929 SAFE CLINIT. D957P-70-100X1 942-892 942-892 2022-12-05 05700699428936 SAFE CLINIT. D957P-70-125X1 942-893 942-893 2022-12-05 05700699428981 SAFE CLINITUBES D957P-70-70X1 942-898 942-898 2024-07-01 05700699429698 safeClinitubes D957P-70-45 942-969 942-969 2022-12-05 05700699440174 QUALICHECK 5+, LEVEL 1 944-017 944-017 2022-12-05 05700699440198 QUALICHECK 5+, LEVEL 3 944-019 944-019 2022-12-05 05700699440822 AUTOCHECK 3+, LEVEL 1, S7335 944-082 944-082 2022-12-05 05700699440839 AUTOCHECK 3+, LEVEL 2, S7345 944-083 944-083 2022-12-05 05700699440846 AUTOCHECK 3+, LEVEL 3, S7355 944-084 944-084 2022-12-05 05700699440853 AUTOCHECK 3+, LEVEL 4, S7365 944-085 944-085 2022-12-05
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