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Henry Schein Safety IV Catheter 26G x 0.75

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
Henry Schein Safety IV Catheter 26G x 0.75 FDA UDI
Generic Name
Intravenous line recessed-needle connector FDA UDI
Device Name
Henry Schein Safety IV Catheter 26G x 0.75 FDA UDI
Model / Reference
HS-843261 FDA UDI
Description
Henry Schein Safety IV Catheter 26G x 0.75 FDA UDI

Identifiers

Primary DI / UDI-DI
00840155406537 FDA UDI
510(k) Number
K131555 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Intravenous line recessed-needle connector

Henry Schein Safety IV Catheter 26G x 0.75 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.

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 99ae4cbc-7302-4eb0-a33a-80ae5ee5043e 34 fields · synced Jun 6, 2026