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XprESS Ultra

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
XprESS Ultra FDA UDI
Generic Name
Eustachian catheter, single-use FDA UDI
Device Name
ENT Dilation System 6x20mm FDA UDI
Model / Reference
MSB&LLF FDA UDI
Description
ENT Dilation System 6x20mm FDA UDI

Identifiers

Catalog Number
ULF-106 FDA UDI
Primary DI / UDI-DI
00857326005123 FDA UDI
FDA Product Code
PNZ FDA UDI
LRC FDA UDI
GMDN Term
Eustachian catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4180 FDA UDI
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Category: Nasal/paranasal balloon catheterEustachian catheter, single-use

XprESS Ultra by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eustachian catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 1c2f8c32-5eb9-4e83-9a71-4d4e81300211 34 fields · synced May 30, 2026