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Injector

FDA UDI

Class II (US FDA UDI)

by Medgyn Products, Inc.

Identity

Trade Name
Injector FDA UDI
Generic Name
Uterine injector FDA UDI
Device Name
EZ Inject HF SHG Catheter FDA UDI
Model / Reference
EZ Inject HF SHG Catheter FDA UDI
Description
EZ Inject HF SHG Catheter FDA UDI

Identifiers

Catalog Number
TMI1162 FDA UDI
Primary DI / UDI-DI
M803TMI1162 FDA UDI
510(k) Number
K032835 FDA UDI
FDA Product Code
LKF FDA UDI
GMDN Term
Uterine injector 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
MRI Safety
MR Safe FDA UDI

Category: Uterine injector

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

Similar devices

Also classified as Uterine injector.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32b3ded0-2e94-45b9-9dbe-5b5f33e43a2a 35 fields · synced Jun 1, 2026