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H/S Catheter

FDA UDI

Class II (US FDA UDI)

by Titus Medical Llc

Identity

Trade Name
H/S Catheter FDA UDI
Generic Name
Uterine injector FDA UDI
Device Name
single unit FDA UDI
Model / Reference
61-50051 FDA UDI
Description
single unit FDA UDI

Identifiers

Primary DI / UDI-DI
B296615005101 FDA UDI
510(k) Number
K092969 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

No

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

No

FDA UDI

Category: Uterine injector

H/S Catheter by Titus Medical Llc — 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

Manufacturer
Titus Medical Llc

Sources (1)

  • FDA UDI 70be869e-cc6a-41b8-bc5e-f7ab3a90ac1c 34 fields · synced Jun 1, 2026