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PALMAZ MULLINS XD Pulmonary Stent

FDA UDI

Class III (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name
PALMAZ MULLINS XD Pulmonary Stent FDA UDI
Generic Name
Bare-metal tracheal/bronchial/vascular stent FDA UDI
Device Name
PALMAZ MULLINS 8F UNEXP L59MM D10MM FDA UDI
Model / Reference
PM5910PXD FDA UDI
Description
PALMAZ MULLINS 8F UNEXP L59MM D10MM FDA UDI

Identifiers

Catalog Number
PM5910PXD FDA UDI
Primary DI / UDI-DI
20705032101223 FDA UDI
PMA Number
P220004 FDA UDI
FDA Product Code
QWC FDA UDI
GMDN Term
Bare-metal tracheal/bronchial/vascular stent FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bare-metal tracheal/bronchial/vascular stent

PALMAZ MULLINS XD Pulmonary Stent by Cordis US Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal tracheal/bronchial/vascular stent.

Cleared under the same submission

P220004 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis US Corp.

Sources (1)

  • FDA UDI 1e0b2c5e-a463-45f6-ae8e-eab8d826e7b0 35 fields · synced May 31, 2026