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Heavy Aspiraton Tubing

FDA UDI

Class II (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
Heavy Aspiraton Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
ASPIRATION TUBING SET FDA UDI
Model / Reference
AT375 FDA UDI
Description
ASPIRATION TUBING SET FDA UDI

Identifiers

Catalog Number
AT375 FDA UDI
Primary DI / UDI-DI
30816989020004 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration tubing set

Heavy Aspiraton Tubing by Hk Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

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 f802b3d5-4588-4b36-8370-37864e089f1a 35 fields · synced May 30, 2026