Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name: ELMED FDA UDI
Generic Name: Body aspiration needle, reusable FDA UDI
Device Name: TITUS VENOCLYSIS NEEDLE, LUER LOCK, 14 GA., BLUNT NEEDLE, 34MM WORKING LENGTH, 3.66MM O.D RETENTION BEAD, 3MM IN LENGTH, 5.75MM FROM THE DISTAL END OF THE NEEDLE, 52.60MM OAL FDA UDI
Model / Reference: TVN-1434B FDA UDI
Description: TITUS VENOCLYSIS NEEDLE, LUER LOCK, 14 GA., BLUNT NEEDLE, 34MM WORKING LENGTH, 3.66MM O.D RETENTION BEAD, 3MM IN LENGTH, 5.75MM FROM THE DISTAL END OF THE NEEDLE, 52.60MM OAL FDA UDI

Identifiers

Catalog Number: TVN-1434B FDA UDI
Primary DI / UDI-DI: 00198506060120 FDA UDI
FDA Product Code: HCD FDA UDI
GMDN Term: Body aspiration needle, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Body aspiration needle, reusable

Elmed by Elmed Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Elmed Incorporated

Sources (1)

FDA UDI 599fc7be-e24a-4f80-831d-5ce9b1cf8ead 35 fields · synced May 31, 2026