Hayden Medical

FDA UDI

Class II (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name: Hayden Medical FDA UDI
Generic Name: Suction system catheter, general-purpose FDA UDI
Device Name: Pynchon Suction Tube 11" (27.5cm), tip with large openings, with removable tubing connection, chrome FDA UDI
Model / Reference: 190-604 FDA UDI
Description: Pynchon Suction Tube 11" (27.5cm), tip with large openings, with removable tubing connection, chrome FDA UDI

Identifiers

Catalog Number: 190-604 FDA UDI
Primary DI / UDI-DI: 00840319741610 FDA UDI
FDA Product Code: JOL FDA UDI
GMDN Term: Suction system catheter, general-purpose FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Suction system catheter, general-purpose

Hayden Medical by Hayden Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I

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 II	Pending data

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Manufacturer

Manufacturer: Hayden Medical Inc

Sources (1)

FDA UDI 5eefbfb4-96ed-44f1-9560-0c2608ac4cd0 35 fields · synced Jun 6, 2026