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Black & Black Surgical, Inc.

FDA UDI

Class II (US FDA UDI)

by Black & Black Surgical, Inc.

Identity

Trade Name
BLACK & BLACK SURGICAL, INC. FDA UDI
Generic Name
Liposuction system FDA UDI
Device Name
AIRSCULPT INFILTRAITON PUMP; LED DISPLAY - VARIABLE SPEED HIGH FLOW FDA UDI
Model / Reference
B86055 FDA UDI
Description
AIRSCULPT INFILTRAITON PUMP; LED DISPLAY - VARIABLE SPEED HIGH FLOW FDA UDI

Identifiers

Catalog Number
B86055 FDA UDI
Primary DI / UDI-DI
00840329834159 FDA UDI
FDA Product Code
QPB FDA UDI
GMDN Term
Liposuction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Liposuction system

Black & Black Surgical, Inc. by Black & Black Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da69ce95-6d0b-4f5e-989a-8195195ba83e 35 fields · synced Jun 1, 2026