Ablation systems
Emprint SX
by Covidien LP
A non-evacuated glass or plastic tube, sealed with a stopper, containing a clot activator and a separator (e.g., gel) to separate blood serum from cells. It is intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation (e.g., blood serum chemistry determinations). This is a single-use device.
Emprint SX models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| CA15L2N | Length 15 cm | MR Unsafe | Available |
| CA20L2N | Length 20 cm | MR Unsafe | Available |
| CA30L2N | Length 30 cm | MR Unsafe | Available |
| CAAL9132 | — | MR Unsafe | Available |
| CAAL9150L | — | MR Unsafe | Available |
| CABK8666L | — | MR Unsafe | Available |
| CABK8816 | — | MR Unsafe | Available |
| CAFG1 | — | Not stated | Available |
| CAFGCART1 | — | Not stated | Available |
| CAFGSP1 | — | Not stated | Available |
| CASYS100 | — | Not stated | Available |
Procedures that use ablation systems
Frequently asked questions
What is Emprint SX used for?
A non-evacuated glass or plastic tube, sealed with a stopper, containing a clot activator and a separator (e.g., gel) to separate blood serum from cells. It is intended to be used for the collection, and preservation and/or transport, of blood for analysis and/or other investigation (e.g., blood serum chemistry determinations). This is a single-use device.
Who makes Emprint SX?
Emprint SX is made by Covidien LP. It is listed under tumor ablation systems (microwave, rf, cryo) in our device library.
What sizes does Emprint SX come in?
Sizes listed for Emprint SX: Length: 15–30 cm. Confirm availability with the manufacturer's instructions for use.
Is Emprint SX MRI safe?
The FDA device database entry for Emprint SX does not state its MRI safety status. Check the labeling before MRI.
Is Emprint SX FDA cleared?
Emprint SX is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Covidien LP sales representative?
Covidien LP has not listed representatives on LA Vascular yet. Visit the Covidien LP company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.