Identity
- Trade Name
- WAL irrigation/aspiration cannula FDA UDI
- Generic Name
- Liposuction system cannula, reusable FDA UDI
- Device Name
- WAL irrigation/aspiration cannula, Ø=4,2mm, 4 Holes, L=30cm, Stainless Steel, Extraction FDA UDI
- Model / Reference
- STS, Ø=4.2, L=300, 4H, Extraction FDA UDI
- Description
- WAL irrigation/aspiration cannula, Ø=4,2mm, 4 Holes, L=30cm, Stainless Steel, Extraction FDA UDI
Identifiers
- Catalog Number
- 503148 FDA UDI
- Primary DI / UDI-DI
- 04260170881229 FDA UDI
- 510(k) Number
- K082025 FDA UDI
- FDA Product Code
- QPB FDA UDI
- GMDN Term
- Liposuction system cannula, reusable 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
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Liposuction system cannula, reusable
WAL irrigation/aspiration cannula by Human Med AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K082025 also covers:
- Biofill Cannula — Human Med AG
- Biofill Cannula — Human Med AG
- Biofill Cannula — Human Med AG
- Biofill Infiltration Cannula — Human Med AG
- Biofill applicator — Human Med AG
- Biofill cannula — Human Med AG
- Biofill cannula — Human Med AG
- Biofill cannula — Human Med AG
- Biofill cannula, RAPID — Human Med AG
- Biofill infiltration cannula — Human Med AG
- Hydrophobic Filter-set — Human Med AG
- Hydrophobic Filter-set — Human Med AG
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Human Med AG
Sources (1)
- FDA UDI 47708091-48fd-400a-85ce-04dea9648e0a 36 fields · synced Jun 6, 2026