Human Med AG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000013901 FEI 3003587189
Human Med AG is a medical device manufacturer based in Germany, with 90 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class IIa and I) and 1 FDA recall as of 13 Nov 2026.
- Devices
- 90
- Registrations
- EUDAMEDFDA
- FDA recalls
- 11 ongoing
Registry facts
- Registries
- FDA GUDID 58
- EUDAMED 56
- FDA 510(k) 2
- Device classes
- FDA Class II 53
- EU Class IIa 28
- FDA Class I 7
- EU Class I 1
- EU Class IIb 1
- Top EMDN categories
- FDA recalls
- Identifiers
- EUDAMED SRN DE-MF-000013901
- FDA FEI 3003587189
- DUNS 332719157
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI, FDA recalls
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.
Catalogue
Search and filter all 90 devicesShowing 1-50 of 90
Company details
- EUDAMED SRN
- DE-MF-000013901
- FDA FEI number
- 3003587189
- DUNS number
- 332719157
- EUDAMED status
- Active
- EUDAMED registered name
- Human Med AG
- Registered address
- 9, Wilhelm-Hennemann-Straße, 19061, Schwerin, Germany
- Website
- www.humanmed.com
- info@humanmed.com
- Phone
- +49 385 395 70 0
- PRRC contact
- Dirk Priewe-Hufmüller
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 28 Apr 2028
DNV MEDCERT GmbH 0482 1 certificate
- 3189GB448260721 Active
Quality management system EU MDR
- Issued
- 21 Jul 2026
- Expires
- 28 Apr 2028
FDA recalls
FDA recall records list 1 recall initiated by Human Med AG, initiated on 2024-10-18. By recorded status: 1 ongoing. The reasons filed fall into these groups: manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 1
- 2025 0
- 2026 0
2024
- 18 Oct 2024 Z-1251-2025 Class II Ongoing The cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spray jet.
Frequently asked questions
How many devices does Human Med AG have in the registry?
The registry currently lists 90 devices for Human Med AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Human Med AG's devices?
Among its 50 most recently registered devices, Human Med AG has devices listed in EUDAMED (40 devices) and FDA GUDID (20 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Human Med AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Human Med AG's devices are Class I, Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Human Med AG?
FDA recall records list 1 recall initiated by Human Med AG, the most recent initiated on 18 Oct 2024. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What EUDAMED certificates are recorded for Human Med AG?
EUDAMED lists 1 certificate for Human Med AG (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 21 Jul 2026.
What are the newest devices from Human Med AG in the registry?
The most recently registered devices listed for Human Med AG include WAL Spül- und Absaugkanüle, body-jet evo, Biofill Applikator and Biofill Kanüle.