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Goldstein

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Goldstein FDA UDI
Generic Name
Intrauterine imaging medium catheter FDA UDI
Device Name
Goldstein Sonohysterography Catheter FDA UDI
Model / Reference
G17149 FDA UDI
Description
Goldstein Sonohysterography Catheter FDA UDI

Identifiers

Catalog Number
J-GSHC-532600 FDA UDI
Primary DI / UDI-DI
00827002171497 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

Goldstein by Cook Incorporated — 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

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 3fa30624-ffc3-411a-bc43-e365c36619aa 36 fields · synced Jun 8, 2026