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Sign in to claim this brandHuman Med AG
US
Last updated May 24, 2026
What Human Med AG makes
Human Med AG manufactures liposuction systems and related components including reusable and single-use cannulas, stromal vascular fraction recovery sets, collection syringe adaptors, surgical irrigation/aspiration tubing sets, tissue injection cannulas, and suction system bottle/canister sealing sets. Their specific devices include extraction cannulas, WAL applicators, Biofill cannulas, FillerCollector devices, and various WAL cannulas for different applications.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI databases. Human Med AG is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What medical devices does Human Med AG manufacture?
Human Med AG specializes in liposuction systems and related components including reusable and single-use cannulas, stromal vascular fraction recovery sets, collection syringe adaptors, surgical tubing sets, tissue injection cannulas, and suction system sealing sets. Their specific products include extraction cannulas, WAL applicators, Biofill cannulas, and FillerCollector devices.
Where is Human Med AG based?
Human Med AG is based in the United States. The company operates within the US market, manufacturing and distributing their medical devices to healthcare professionals and facilities throughout the country.
Which regulatory registries list Human Med AG's devices?
Human Med AG's devices are listed in the FDA 510(k) database and the FDA UDI (Unique Device Identification) database. These registries track medical devices that have been submitted for clearance or are marketed in the United States.
How are Human Med AG's devices classified?
Human Med AG's medical devices are classified as Class I and Class II devices under the FDA regulatory framework. Class I devices are low-risk and subject to general controls, while Class II devices require special controls in addition to general controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- humanmed.com
- —
- —
- [email protected]
- Phone
- +49385395700
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 332719157
Catalogue (60)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Disposable Set LipoCollector III | Single-use Disposable Set for Re-usable LipoCollector III | FDA UDI | Class II | Active |
| STS Adapter, 5cm | STS Adapter, for WAL Applicator Short and Biofill Cannula, L=50 | FDA UDI | Class II | Active |
| WAL infiltration cannula | STS, Ø2,5mm, L=300, 0H, Infiltration | FDA UDI | Class II | Active |
| WAL irrigation/aspiration cannula | STS, Ø=4.8, L=300, 4H, Extraction | FDA UDI | Class II | Active |
| Biofill cannula | STS, Ø=3.0, L=150, 2H, Extraction | FDA UDI | Class II | Active |
| WAL Infiltration Cannula | Single-use, Ø=2.5, L=200, 0H, 180°, Infiltration | FDA UDI | Class II | Active |
| BEAULI Infiltration cannula | Single-use BEAULI Infiltration Cannula, Ø=2 | FDA UDI | Class I | Active |
| Hydrophobic Filter-set | Hydrophobic Filter-set for Q-graft control | FDA UDI | Class II | Active |
| Body-Jet | K082025 | FDA 510(k) | Class II | Active |
| Lipcollector Ii | K101713 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Human Med Ag SCHWERIN Mecklenburg-Western Pomerania · DE FEI 3003587189