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WAL Infiltration Cannula

FDA UDI

Class II (US FDA UDI)

by Human Med AG

Identity

Trade Name
WAL Infiltration Cannula FDA UDI
Generic Name
Liposuction system cannula, single-use FDA UDI
Device Name
WAL Infiltration Cannula, Ø=2,5mm, L=30cm, 0 Holes, Single-use, Infiltration FDA UDI
Model / Reference
Single-use, Ø=2.5, L=300, 0H, Infiltration FDA UDI
Description
WAL Infiltration Cannula, Ø=2,5mm, L=30cm, 0 Holes, Single-use, Infiltration FDA UDI

Identifiers

Catalog Number
1500127-5 FDA UDI
Primary DI / UDI-DI
04260170880840 FDA UDI
510(k) Number
K082025 FDA UDI
FDA Product Code
QPB FDA UDI
GMDN Term
Liposuction system cannula, single-use 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Liposuction system cannula, single-use

WAL Infiltration Cannula by Human Med AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Human Med AG

Sources (1)

  • FDA UDI 077e99d6-4635-4a34-86cd-57047eb2ba50 37 fields · synced May 30, 2026