User's Manual
Table Of Contents
- Intended Use
- Prior to Installation
- Installation
- Child Safety
- During Use
- Maintenance and Cleaning
- Servicing
- Disposing of the FROSTMED
- Handling of CO2
- CO2 Canister Transportation
- CO2Temperature
- CO2 Pressure
- CO2 Refilling Process
- CO2 Canister Storage and Transportation (empty/full)
- In the very rare case of a frostbite
- IC and FCC Compliance
- This device complies with Industry Canada license-exempt RSS standard(s). This device complies with Part 15 of the FCC rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device...
- FCC/ISED RF exposure
- This equipment complies with FCC radiation exposure limits and Canada radiation RF exposure limits set forth in CFR 47 Sections 2.1091 and Industry Canada RSS-102 for an uncontrolled environment. This equipment should be installed and operated with a ...
- FCC Caution: Any changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate this equipment.
- Digital class B notice
- NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential insta...
- • Reorient or relocate the receiving antenna.
- • Increase the separation between the equipment and receiver.
- • Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
- • Consult the dealer or an experienced radio/TV technician for help.
- FDA clearance
- FROSTMED devices (PRO G1, PRO G2, LITE G1, LITE G2, LITE CV G1 and LITE CV G2 models) are
- FDA-cleared as Class II device, 510(K) exempts.
- 1. Introduction
- 2. Starting FROSTMED PRO, LITE, LITE CV
- 3. Operating FROSTMED
- 4. Removing Empty CO2 Canisters
- 5. Alert Programming and Notification
- 6. Troubleshoot
- 7. Service and Spare Parts
- 8. Customer Service Department
- Informations importantes relatives à la sécurité
- Utilisation prévue
- Avant l’installation
- Installation
- Sécurité des enfants
- Pendant l’utilisation
- Entretien et nettoyage
- Réparations
- Élimination de FROSTMED
- Manipulation du CO2
- Transport des cartouches de CO2
- Température du CO2
- Pression du CO2
- Processus de remplissage des cartouches de CO2
- Stockage et transport des cartouches de CO2 (vides/pleines)
- Dans les très rares cas d’engelures
- Conformité
- Informations importantes relatives à la sécurité
- 1. Introduction
- 2. Commencer à utiliser FROSTMED PRO, LITE, LITE CV
- 3. Fonctionnement de FROSTMED
- 4. Retrait des cartouches de CO2 vides
- 5. Programmation et notification des alertes
- 6. Dépannage
- 7. Réparation et pièces de rechange
- 8. Service client
2) select the biological product to be transported (Figure 7). In this case FROSTMED
automatically set the temperature according to the following temperature ranges:
a. Blood:
• Min: +1°C
• Max: +10°C
• Setpoint: +°4C
b. Platelets:
• Min: +18°C
• Max: +24°C
• Setpoint: +21°C
c. Sample:
• Min: +12°C
• Max: +20°C
• Setpoint: +15°C
d. Vaccines
• Min: +2°C
• Max: +8°C
• Setpoint: +5°C
e. Insulin
• Min: +2°C
• Max: +8°C
• Setpoint: +5°C
f. Corneas
• Min: -8°C
• Max: +2°C
• Setpoint: -3°C
g. Room temperature specimens
• Min: +20°C
• Max: +25°C
• Setpoint: +23°C
h. Refrigerated specimens
• Min: +4°C
• Max: +8°C
• Setpoint: +6°C
i. Manual
If none of the above range applies to your desired temperature range, please use option 1).
To get back to option 1), if currently using a content type, select content type “i. Manual” from
the list of content types.