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MedSource Catheters

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Catheters FDA UDI
Generic Name
Intravenous line recessed-needle connector FDA UDI
Device Name
TrueSafe Blood Control 16G x 1.77” FDA UDI
Model / Reference
MS-86316 FDA UDI
Description
TrueSafe Blood Control 16G x 1.77” FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00840155409361 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

MedSource 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 dbacd816-ea22-4a4a-925b-4b7f0e2a8769 34 fields · synced Jun 8, 2026