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Hysterosalpingography (HSG) Catheter

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Hysterosalpingography (HSG) Catheter FDA UDI
Generic Name
Intrauterine imaging medium catheter FDA UDI
Device Name
Hysterosalpingography (HSG) Catheter 7Fr x 40cm FDA UDI
Model / Reference
660007040 FDA UDI
Description
Hysterosalpingography (HSG) Catheter 7Fr x 40cm FDA UDI

Identifiers

Catalog Number
660007040 FDA UDI
Primary DI / UDI-DI
00886333001170 FDA UDI
FDA Product Code
LKF FDA UDI
GMDN Term
Intrauterine imaging medium catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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

Category: Intrauterine imaging medium catheter

Hysterosalpingography (HSG) Catheter by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intrauterine imaging medium catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 333bf83c-96b9-4251-9cd0-78a52f56ae08 37 fields · synced Jun 9, 2026