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Smith's Catheters

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
Smith's Catheters FDA UDI
Generic Name
Intravenous line recessed-needle connector FDA UDI
Device Name
Truesafe (PTFE Catheter), 14G x 1.75" FDA UDI
Model / Reference
SM-84414 FDA UDI
Description
Truesafe (PTFE Catheter), 14G x 1.75" FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00840155410749 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Intravenous line recessed-needle connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

No

FDA UDI

Category: Intravenous line recessed-needle connector

Smith's Catheters by Medsource International Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous line recessed-needle connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medsource International Llc

Sources (1)

  • FDA UDI 4cad717a-0386-4b61-836d-e2a402032961 34 fields · synced May 30, 2026