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MedGyn IUI catheter

FDA UDI

Class II (US FDA UDI)

by Medgyn Products, Inc.

Identity

Trade Name
MedGyn IUI catheter FDA UDI
Generic Name
Sperm filtration system FDA UDI
Device Name
Insemination catheter FDA UDI
Model / Reference
straight iui FDA UDI
Description
Insemination catheter FDA UDI

Identifiers

Catalog Number
022723 FDA UDI
Primary DI / UDI-DI
M803022723 FDA UDI
FDA Product Code
MQF FDA UDI
GMDN Term
Sperm filtration system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6110 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Sperm filtration system

MedGyn IUI catheter by Medgyn Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sperm filtration system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medgyn Products, Inc.

Sources (1)

  • FDA UDI ebd84d25-0f2f-4c16-b2a0-9c6f02e16fe3 34 fields · synced May 30, 2026