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Propel

FDA UDI

Class III (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
PROPEL FDA UDI
Generic Name
Drug-eluting paranasal sinus stent FDA UDI
Device Name
IMPLANT 60011 PROPEL MINI FDA UDI
Model / Reference
60011 FDA UDI
Description
IMPLANT 60011 PROPEL MINI FDA UDI

Identifiers

Primary DI / UDI-DI
00763000710330 FDA UDI
PMA Number
P100044 FDA UDI
FDA Product Code
OWO FDA UDI
GMDN Term
Drug-eluting paranasal sinus 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Drug-eluting paranasal sinus stent

Propel by Medtronic Xomed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Drug-eluting paranasal sinus stent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae0b511f-8af1-4409-ad99-459ad69b6b8f 36 fields · synced May 30, 2026