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Disposable Micro Cannula For Filler Injection Kit

FDA UDI

Class I (US FDA UDI)

by Aesthetic Group

Identity

Trade Name
DISPOSABLE MICRO CANNULA FOR FILLER INJECTION KIT FDA UDI
Generic Name
Tissue injection cannula FDA UDI
Device Name
21gauge x 7 cm - 1-hole FDA UDI
Model / Reference
1-hole FDA UDI
Description
21gauge x 7 cm - 1-hole FDA UDI

Identifiers

Catalog Number
MI2170KS FDA UDI
Primary DI / UDI-DI
03701068805305 FDA UDI
510(k) Number
K132353 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Tissue injection cannula 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

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 Micro Cannula For Filler Injection Kit by Aesthetic Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue injection cannula.

Cleared under the same submission

K132353 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesthetic Group

Sources (1)

  • FDA UDI 50d0af4d-8697-4d36-9cbb-3a7c43937ea8 36 fields · synced May 30, 2026