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Accelerator III 3mm x 23cm Luer Lock Cannula

FDA UDI

Class II (US FDA UDI)

by Mentor Texas LP

Identity

Trade Name
Accelerator III 3mm x 23cm Luer Lock Cannula FDA UDI
Generic Name
Liposuction system cannula, reusable FDA UDI
Device Name
Accelerator III 3mm x 23cm Luer Lock Cannula FDA UDI
Model / Reference
BNIII323 FDA UDI
Description
Accelerator III 3mm x 23cm Luer Lock Cannula FDA UDI

Identifiers

Catalog Number
BNIII323 FDA UDI
Primary DI / UDI-DI
00081317020790 FDA UDI
510(k) Number
K981172 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Liposuction system cannula, reusable 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

Accelerator III 3mm x 23cm Luer Lock Cannula by Mentor Texas LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mentor Texas LP

Sources (1)

  • FDA UDI a56fd785-97c1-47ac-99ca-e24bd780c880 36 fields · synced May 31, 2026