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Double Spike Infiltration Tubing

FDA UDI

Class I (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
Double Spike Infiltration Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
INFILTRATION TUBING SET FDA UDI
Model / Reference
ITD-20 FDA UDI
Description
INFILTRATION TUBING SET FDA UDI

Identifiers

Catalog Number
ITD-20 FDA UDI
Primary DI / UDI-DI
38169890200082 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Double Spike Infiltration Tubing by Hk Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 444fa9c6-7f7c-428c-b04d-c3e3a6d942ec 36 fields · synced May 31, 2026