Biliary drains

Palmaz Genesis

by Cordis US Corp.

A non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency; it is not intended for vascular implantation. It may be a mesh structure or a continuous tube and is made entirely of metal [e.g., high-grade stainless steel, cobalt-chrome (Co-Cr), nickel-titanium alloy (Nitinol)]. It may be expandable in situ (e.g., with a balloon catheter or self-expands) and disposable devices intended to assist implantation may be included.

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Where to buy Palmaz Genesis

Contact Cordis US Corp. directly; they can quote, ship, or point you to the distributor for your country.

From cordis.com, 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.

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Palmaz Genesis models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
PG124Bβ€” MR ConditionalAvailable
PG124Pβ€” MR ConditionalAvailable
PG154Bβ€” MR ConditionalAvailable
PG184Bβ€” MR ConditionalAvailable
PG184Pβ€” MR ConditionalAvailable
PG244Bβ€” MR ConditionalAvailable
PG295Bβ€” MR ConditionalAvailable
PG295Pβ€” MR ConditionalAvailable
PG395Bβ€” MR ConditionalAvailable
PG395Pβ€” MR ConditionalAvailable
PG595Bβ€” MR ConditionalAvailable
PG595Pβ€” MR ConditionalAvailable
PG795Bβ€” MR ConditionalAvailable
PG1910Bβ€” MR ConditionalAvailable
PG2510Bβ€” MR ConditionalAvailable
PG2910Bβ€” MR ConditionalAvailable
PG3910Bβ€” MR ConditionalAvailable
PG5910Bβ€” MR ConditionalAvailable

FDA clearances

  • 510(k) K020809 April 2002
  • 510(k) K012090 August 2001
  • 510(k) K012087 August 2001

Procedures that use biliary drains

Frequently asked questions

What is Palmaz Genesis used for?

A non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency; it is not intended for vascular implantation. It may be a mesh structure or a continuous tube and is made entirely of metal [e.g., high-grade stainless steel, cobalt-chrome (Co-Cr), nickel-titanium alloy (Nitinol)]. It may be expandable in situ (e.g., with a balloon catheter or self-expands) and disposable devices intended to assist implantation may be included.

Who makes Palmaz Genesis?

Palmaz Genesis is made by Cordis US Corp.. It is listed under biliary drainage catheters in our device library.

What sizes does Palmaz Genesis come in?

The FDA device database does not list sizes for Palmaz Genesis. Check the instructions for use or ask a Cordis US Corp. representative.

Is Palmaz Genesis MRI safe?

The FDA device database lists Palmaz Genesis as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Palmaz Genesis FDA cleared?

Palmaz Genesis is covered by FDA submissions K012087, K012090, K020809.

How do I contact a Cordis US Corp. sales representative?

Cordis US Corp. has not listed representatives on LA Vascular yet. Visit the Cordis US Corp. 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.

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