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WAL Cannula

FDA UDI

Class II (US FDA UDI)

by Human Med AG

Identity

Trade Name
WAL Cannula FDA UDI
Generic Name
Liposuction system cannula, single-use FDA UDI
Device Name
WAL Cannula, Ø=4.8mm, 8 Holes, Rapid, L=30cm, Single-use, Extraction FDA UDI
Model / Reference
Single-use, Ø=4.8, L=300, 8H, Extraction FDA UDI
Description
WAL Cannula, Ø=4.8mm, 8 Holes, Rapid, L=30cm, Single-use, Extraction FDA UDI

Identifiers

Catalog Number
1503005-5 FDA UDI
Primary DI / UDI-DI
04260170880963 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 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 4e0e8ecb-29fe-444d-80e0-3f87f8b36fc8 37 fields · synced May 30, 2026