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Fine Touch Aspiration Tubing

FDA UDI

Class II (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
Fine Touch Aspiration Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
FINE TOUCH ASPIRATION TUBING FDA UDI
Model / Reference
ATF-20 FDA UDI
Description
FINE TOUCH ASPIRATION TUBING FDA UDI

Identifiers

Catalog Number
ATF-20 FDA UDI
Primary DI / UDI-DI
30816989020028 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Fine Touch Aspiration Tubing by Hk Surgical Inc. — Class II — 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 3f968c89-0d0c-42fb-9b6e-4b83e99b9e7c 36 fields · synced May 31, 2026