Dr. Arabin GmbH & Co. KG
Germany Last updated 17 Sep 2026
- Devices
- 155
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Sp 085 Ref SP 085
Cpp 65/25/32 Ref CPP 65/25/32
Kp 055 Ref KP 055
Up 060 Ref UP 060
Cpp 70/17/35 Ref CPP 70/17/35
Ahypn 065 Ref AHYPN 065
Ssp 095 Ref SSP 095
TP1+1 F1 Ref TP1+1 F1
TP1+2 F1 Ref TP1+2 F1
Cpp 70/25/32 Ref CPP 70/25/32
Upm 050 Ref UPM 050
Hp 075 Ref HP 075
Rp 100 Ref RP 100
Ahypn 075 Ref AHYPN 075
TPP4+5 F4 Ref TPP4+5 F4
TPP3+3 F3 Ref TPP3+3 F3
Up 085 Ref UP 085
Ahypns 070 Ref AHYPNS 070
TPP1+1 F1 Ref TPP1+1 F1
Ahypn 080 Ref AHYPN 080
Rp 060 Ref RP 060
Usp 065 Ref USP 065
Sp 070 Ref SP 070
Upm 065 Ref UPM 065
Ahypns 075 Ref AHYPNS 075
Sp 095 Ref SP 095
TP3+3 F3 Ref TP3+3 F3
Rp 055 Ref RP 055
Cpp 70/21/35 Ref CPP 70/21/35
TP5+5 F5 Ref TP5+5 F5
Ahypns 065 Ref AHYPNS 065
Ssp 080 Ref SSP 080
Ssp 060 Ref SSP 060
Wpp 1 Ref WPP 1
Up 100 Ref UP 100
Rp 090 Ref RP 090
Up 045 Ref UP 045
Upm 045 Ref UPM 045
Ssp 070 Ref SSP 070
Wpp 4 Ref WPP 4
Upm 060 Ref UPM 060
Usp 075 Ref USP 075
TPP2+2 F2 Ref TPP2+2 F2
Ahypns 060 Ref AHYPNS 060
Rp 065 Ref RP 065
Wp 4 Ref WP 4
Wpp 2 Ref WPP 2
Upm 095 Ref UPM 095
Hp 085 Ref HP 085
Wp 6 Ref WP 6
Showing 1-50 of 155
EUDAMED certificates
Notified body 0482 1 certificate
- 1340GB448241217 Issued
Quality management system EU MDR
- Issued
- 17 Dec 2024
- Expires
- 2 Jul 2028
Related companies
Notified bodies
- Notified body 0482
What Dr. Arabin GmbH & Co. KG makes
Dr. Arabin GmbH & Co. KG manufactures a range of medical devices primarily used in obstetrics and gynecology, including cervical dilators (e.g., SP 085, CPP series), intrauterine pressure catheters (e.g., UPM 050, UP 060), and fetal monitoring systems (e.g., TP1+1 F1, TP1+2 F1). Their portfolio also includes devices for uterine pressure measurement (e.g., HP 075) and specialized obstetric tools (e.g., AHYPN 065, SSP 095, KP 055).
The company’s devices are classified under EU regulations as Class IIa and Class IIb, indicating moderate to high risk, and are registered in the EU’s medical device database, eudamed. The manufacturer is based in Germany and adheres to EU regulatory requirements for medical device compliance.
Frequently asked questions
How many devices does Dr. Arabin GmbH & Co. KG have in the registry?
The registry currently lists 155 devices for Dr. Arabin GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Arabin GmbH & Co. KG's devices?
Among its 50 most recently registered devices, Dr. Arabin GmbH & Co. KG has devices listed in EUDAMED (50 devices).
What risk classes do Dr. Arabin GmbH & Co. KG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Dr. Arabin GmbH & Co. KG's devices are Class IIa and Class IIb. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Dr. Arabin GmbH & Co. KG?
EUDAMED lists 1 certificate for Dr. Arabin GmbH & Co. KG (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 2024-12-17.
What are the newest devices from Dr. Arabin GmbH & Co. KG in the registry?
The most recently registered devices listed for Dr. Arabin GmbH & Co. KG include SP 085, CPP 65/25/32, KP 055 and UP 060.
Information
- Address
- 44, Alfred-Herrhausen-Straße , Witten, Germany
- Website
- www.dr-arabin.de
- [email protected]
- Phone
- +49 2302189214
- PRRC contact
- Birgit Arabin
- EUDAMED SRN
- DE-MF-000005474