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Infiltration kit

FDA UDI

Class I (US FDA UDI)

by Aesthetic Group

Identity

Trade Name
Infiltration kit FDA UDI
Generic Name
Autologous adipose tissue reinjection set FDA UDI
Device Name
This kit is a convenience kit. The devices contained in the infiltration kit are used to collect fat tissue. The procedure usually involves infiltration of tumescent solution before harvesting fat tissue by liposuction. FDA UDI
Model / Reference
1 FDA UDI
Description
This kit is a convenience kit. The devices contained in the infiltration kit are used to collect fat tissue. The procedure usually involves infiltration of tumescent solution before harvesting fat tissue by liposuction. FDA UDI

Identifiers

Catalog Number
PACK001-BI FDA UDI
Primary DI / UDI-DI
03760173233694 FDA UDI
FDA Product Code
FTN FDA UDI
GMDN Term
Autologous adipose tissue reinjection set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3925 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Autologous adipose tissue reinjection set

Infiltration kit by Aesthetic Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autologous adipose tissue reinjection set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesthetic Group

Sources (1)

  • FDA UDI abbcd198-4a9f-4ce3-9dc5-ba86976aa538 35 fields · synced May 30, 2026