Aesculap Chifa Sp. z o.o.
Active in EUDAMEDPolandfrom SRN EUDAMED FDA SRN PL-MF-000002120 FEI 3002315844
- Devices
- 21
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
2 of 2 in force.
Market reach
- European Union
- EUDAMED actor, 2 certificates
- United States
- FDA establishment
Catalogue
Search and filter all 21 devicesCompany details
- EUDAMED SRN
- PL-MF-000002120
- FDA FEI number
- 3002315844
- EU VAT number
- PL7880008829
- EUDAMED status
- Active
- EUDAMED registered name
- Aesculap Chifa Sp. z o.o.
- Registered address
- 14, Tysiąclecia, 64-300, Nowy Tomyśl, Poland
- Website
- www.bbraun.com
- linkedin.com/company/6773
- facebook.com/bbrauninternational
- [email protected]
- PRRC contact
- Mateusz Hoffmann
EUDAMED certificates
2 certificates2 valid, 0 expiredMDR 2next expiry 8 Nov 2026
TÜV SÜD Product Service GmbH 0123 2 certificates
- G11 038951 0012 Reissued
Quality management system EU MDR
- Issued
- 15 Sep 2026
- Expires
- 8 Nov 2031
- Valid from
- 9 Nov 2026
- G11 038951 0012 Issued
Quality management system EU MDR
- Issued
- 9 Nov 2021
- Expires
- 8 Nov 2026
FDA establishments
- Aesculap Chifa Sp Z O O US
From the company website
B. Braun offers medical equipment as well as health care solutions across a wide range of applications.
Frequently asked questions
How many devices does Aesculap Chifa Sp. z o.o. have in the registry?
The registry currently lists 21 devices for Aesculap Chifa Sp. z o.o.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aesculap Chifa Sp. z o.o.'s devices?
Among its 21 most recently registered devices, Aesculap Chifa Sp. z o.o. has devices listed in EUDAMED (21 devices).
What risk classes do Aesculap Chifa Sp. z o.o.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Aesculap Chifa Sp. z o.o.'s devices are Class I. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Aesculap Chifa Sp. z o.o.?
EUDAMED lists 2 certificates for Aesculap Chifa Sp. z o.o. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 2026-09-15.
What are the newest devices from Aesculap Chifa Sp. z o.o. in the registry?
The most recently registered devices listed for Aesculap Chifa Sp. z o.o. include Chifa.
Which FDA establishments are linked to Aesculap Chifa Sp. z o.o.?
1 FDA establishment is linked to Aesculap Chifa Sp. z o.o. in the registry; they are listed on the company page.