LiNA Medical AG
Active in EUDAMEDSwitzerlandfrom SRN EUDAMED FDA SRN CH-MF-000046832 FEI 3008693678
- Devices
- 136
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
What LiNA Medical AG makes
LiNA Medical AG manufactures single-use surgical and procedural accessories, including sterile containment bags for laparoscopic instruments and surgical tools, such as the LiNA EasyBag and Brenner Medical Lap-Bag. Their portfolio also includes reusable port protection devices like the LiNA Port, as well as sterile wipes like the LiNA Clear Sight Wipe for preoperative site preparation. Additional products like the LiNA EndoBag and LiNA LapGuard are designed for endoscopic and laparoscopic procedures, ensuring sterile environments and instrument protection. The company also produces the LiNA SeaStar, a device for managing and securing surgical instruments during procedures.
The company’s devices are classified under EU regulations as Class I, Class IIa, and Class IIb, with all products listed in the EU’s eudamed database. These classifications reflect varying levels of risk and regulatory oversight, from low-risk items like wipes and reusable ports to higher-risk surgical containment systems. LiNA Medical AG is headquartered in Switzerland and adheres to EU medical device compliance requirements for market placement.
Catalogue
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Company details
- EUDAMED SRN
- CH-MF-000046832
- FDA FEI number
- 3008693678
- DUNS number
- 485705870
- EUDAMED status
- Active
- EUDAMED registered name
- LiNA Medical AG
- Registered address
- 3, Platz, 6039, Root D4, Switzerland
- Website
- linamed.com/
- [email protected]
- Phone
- +48 789 105 422
- PRRC contact
- Paweł Łukaszewicz
EUDAMED certificates
2 certificates1 valid, 0 expired, 1 withdrawn or suspendedMDR 2next expiry 19 Feb 2031
TUV NORD Polska Sp. z o.o 2274 1 certificate
- TNP/MDR/0050/5851/2026 Cancelled
Quality management system EU MDR
- Issued
- 20 Feb 2026
- Expires
- 19 Feb 2031
- Reason
- Other
TÜV Rheinland LGA Products GmbH 0197 1 certificate
- HZ 2745863-1 Active
Quality management system EU MDR
- Issued
- 5 Aug 2026
- Expires
- 19 Feb 2031
- Reason
- Add device or group