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HK Connector for Safety Syringe

FDA UDI

Class I (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
HK Connector for Safety Syringe FDA UDI
Generic Name
Liposuction system cannula, reusable FDA UDI
Device Name
HK Connector for Safety Syringe FDA UDI
Model / Reference
HKCONFSS FDA UDI
Description
HK Connector for Safety Syringe FDA UDI

Identifiers

Catalog Number
HKCONFSS FDA UDI
Primary DI / UDI-DI
00816989020706 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

HK Connector for Safety Syringe by Hk Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hk Surgical Inc.

Sources (1)

  • FDA UDI df31724a-5a75-4764-8654-caf1d93a10f7 35 fields · synced May 30, 2026