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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Paranasal sinus irrigation catheter FDA UDI
Device Name
TRAP,MUCUS SPECIMEN, 80CC FDA UDI
Model / Reference
DYND44180 FDA UDI
Description
TRAP,MUCUS SPECIMEN, 80CC FDA UDI

Identifiers

Catalog Number
DYND44180 FDA UDI
Primary DI / UDI-DI
10080196818624 FDA UDI
FDA Product Code
BYZ FDA UDI
GMDN Term
Paranasal sinus irrigation catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Paranasal sinus irrigation catheter

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Paranasal sinus irrigation catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 685c78ef-dfb3-4f17-a605-60d612794ad7 35 fields · synced Jun 8, 2026