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Multi-Hole Cannula

FDA UDI

Class I (US FDA UDI)

by Möller Medical GmbH

Identity

Trade Name
Multi-Hole Cannula FDA UDI
Generic Name
Liposuction system cannula, single-use FDA UDI
Model / Reference
ASC-S311-50-0350 FDA UDI

Identifiers

Primary DI / UDI-DI
04260277179908 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Liposuction system cannula, single-use 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Liposuction system cannula, single-use

Multi-Hole Cannula by Möller Medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81f9c5d7-5120-4e40-a9d3-f56c082347ee 32 fields · synced Jun 9, 2026