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Aspiration Handle-Aluminum Large 1" diameter

FDA UDI

Class I (US FDA UDI)

by Hk Surgical Inc.

Identity

Trade Name
Aspiration Handle-Aluminum Large 1" diameter FDA UDI
Generic Name
Liposuction system cannula, reusable FDA UDI
Device Name
Aspiration Handle-Aluminum Large 1" diameter FDA UDI
Model / Reference
AHL FDA UDI
Description
Aspiration Handle-Aluminum Large 1" diameter FDA UDI

Identifiers

Catalog Number
AHL FDA UDI
Primary DI / UDI-DI
00816989020669 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

Aspiration Handle-Aluminum Large 1" diameter 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 8087b3f4-03a5-4a25-b3ad-442460a9966e 35 fields · synced Jun 8, 2026