HK Connector Standard Luer Lock

FDA UDI

Class I (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name: HK Connector Standard Luer Lock FDA UDI
Generic Name: Liposuction system cannula, reusable FDA UDI
Device Name: HK Connector Standard Luer Lock FDA UDI
Model / Reference: HKCONSLL FDA UDI
Description: HK Connector Standard Luer Lock FDA UDI

Identifiers

Catalog Number: HKCONSLL FDA UDI
Primary DI / UDI-DI: 00816989020713 FDA UDI
FDA Product Code: GEA FDA UDI
GMDN Term: Liposuction system cannula, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

HK Connector Standard Luer Lock by Hk Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Canules réutilisables / Reusable cannulas — Euromi · Class IIa

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: Hk Surgical Inc.

Sources (1)

FDA UDI bec59cf5-d3a7-4c41-a999-972653b975fc 35 fields · synced May 30, 2026