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Disposable Tumescent Infiltration Cannula

FDA UDI

Class II (US FDA UDI)

by Aesthetic Group

Identity

Trade Name
DISPOSABLE TUMESCENT INFILTRATION CANNULA FDA UDI
Generic Name
Tissue injection cannula FDA UDI
Device Name
2,5mm x 25 cm - 10-hole FDA UDI
Model / Reference
10-hole FDA UDI
Description
2,5mm x 25 cm - 10-hole FDA UDI

Identifiers

Catalog Number
CI25250 FDA UDI
Primary DI / UDI-DI
03701068800829 FDA UDI
510(k) Number
K132353 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Tissue injection cannula 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue injection cannula

Disposable Tumescent Infiltration Cannula by Aesthetic Group — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue injection cannula.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesthetic Group

Sources (1)

  • FDA UDI d393dd72-b49e-48b4-a9b4-6cd2c76c810c 36 fields · synced May 30, 2026