Medinux (Tianjin) Technologies Co., Ltd.
Active in EUDAMEDChinafrom SRN EUDAMED FDA SRN CN-MF-000048891 FEI 3030529508
- Devices
- 35
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
What Medinux (Tianjin) Technologies Co., Ltd. makes
Medinux (Tianjin) Technologies Co., Ltd. manufactures the CryoThin™ Surgical System and its associated accessories, which are designed for cryosurgical procedures. These devices utilize controlled freezing techniques to treat tissue, commonly used in dermatology and other surgical applications.
The company’s products fall under Class II regulatory classification in the US, with the CryoThin™ Surgical System and Accessories authorised through the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Search and filter all 35 devicesCompany details
- EUDAMED SRN
- CN-MF-000048891
- FDA FEI number
- 3030529508
- DUNS number
- 725612588
- EUDAMED status
- Active
- EUDAMED registered name
- Medinux (Tianjin) Technologies Co., Ltd.
- EUDAMED abbreviated name
- Medinux
- Registered address
- No.6 Haitai Fazhan 6th Road, 300384, Tianjin, China
- Website
- www.medinux.com
- [email protected]
- Phone
- +86 22 8639 2536
- PRRC contact
- DIANA ZHANG
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 2 Aug 2031
IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. 0051 1 certificate
- 307/MDR Active
Quality management system EU MDR
- Issued
- 3 Aug 2026
- Expires
- 2 Aug 2031
Frequently asked questions
How many devices does Medinux (Tianjin) Technologies Co., Ltd. have in the registry?
The registry currently lists 35 devices for Medinux (Tianjin) Technologies Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medinux (Tianjin) Technologies Co., Ltd.'s devices?
Among its 35 most recently registered devices, Medinux (Tianjin) Technologies Co., Ltd. has devices listed in EUDAMED (23 devices), FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Medinux (Tianjin) Technologies Co., Ltd.'s devices fall under?
Among its 35 most recently registered devices, the classes recorded for Medinux (Tianjin) Technologies Co., Ltd.'s devices are Class IIb and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Medinux (Tianjin) Technologies Co., Ltd.?
EUDAMED lists 1 certificate for Medinux (Tianjin) Technologies Co., Ltd. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 3 Aug 2026.
What are the newest devices from Medinux (Tianjin) Technologies Co., Ltd. in the registry?
The most recently registered devices listed for Medinux (Tianjin) Technologies Co., Ltd. include 2.1 mm Outer CryoE Probe (Sleeve), Cryoelectric Ablation System (8-port Standard Console), 1.2 mm Variable CryoE Probe and 1.0 mm Electrode (TP Probe).