Biliary drains
Endoflux
A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency. It is made entirely of a synthetic polymer(s) [e.g., polytetrafluoroethylene (PTFE), polyethylene (PE), silicone] and may have various designs (e.g., continuous tube with or without drainage side holes, covered or non-covered mesh structure). Disposable devices intended to assist implantation may be included.
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Where to buy Endoflux
Contact Medi-Globe GmbH directly; they can quote, ship, or point you to the distributor for your country.
From mediglobe-endoflex.de, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Endoflux 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 |
|---|---|---|---|
| GBS-01-07-004 | Length 4 cm | MR Safe | Available |
Procedures that use biliary drains
Frequently asked questions
What is Endoflux used for?
A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency. It is made entirely of a synthetic polymer(s) [e.g., polytetrafluoroethylene (PTFE), polyethylene (PE), silicone] and may have various designs (e.g., continuous tube with or without drainage side holes, covered or non-covered mesh structure). Disposable devices intended to assist implantation may be included.
Who makes Endoflux?
Endoflux is made by Medi-Globe GmbH. It is listed under biliary drainage catheters in our device library.
What sizes does Endoflux come in?
Sizes listed for Endoflux: Length: 4 cm. Confirm availability with the manufacturer's instructions for use.
Is Endoflux MRI safe?
The FDA device database lists Endoflux as MR Safe. Always follow the specific MRI conditions in the labeling.
Is Endoflux FDA cleared?
Endoflux is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Medi-Globe GmbH sales representative?
Medi-Globe GmbH has not listed representatives on LA Vascular yet. Visit the Medi-Globe GmbH 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.