PAR Medizintechnik GmbH & Co. KG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000017480 FEI 3001744144
- Devices
- 3
- 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 PAR Medizintechnik GmbH & Co. KG makes
PAR Medizintechnik GmbH & Co. KG manufactures blood pressure measurement devices, including the TONOPORT VI—a non-invasive oscillometric blood pressure monitor—and disposable blood pressure cuffs in large and medium sizes with D-ring attachments for secure fitting. These products are designed for clinical and home use to measure systolic and diastolic blood pressure accurately.
The company’s devices are classified under EU Class I and Class II regulations, with listings in the EUDAMED database and FDA’s 510(k) registry. The manufacturer is based in Germany, adhering to European and U.S. medical device compliance requirements.
Catalogue
Tonoport Vi Ref K170966
Regimes: CE MDR 510(k) Registry: EUDAMED510(k)GUDIDLZBD Cuff Large mit D-Ring Ref A2500-l
Regimes: CE MDR Registry: EUDAMEDLZBD Cuff Medium mit D-Ring Ref A2500-m
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000017480
- FDA FEI number
- 3001744144
- EU VAT number
- DE 136639104
- EUDAMED status
- Active
- EUDAMED registered name
- PAR Medizintechnik GmbH & Co. KG
- EUDAMED abbreviated name
- PAR
- Registered address
- 11, Rigistr., 12277, Berlin, Germany
- Website
- www.par-berlin.com
- [email protected]
- PRRC contact
- Bülent Tek
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 26 Jan 2027
DNV MEDCERT GmbH 0482 1 certificate
- 2210GB448240301 Expiring
Quality management system EU MDR
- Issued
- 1 Mar 2024
- Expires
- 26 Jan 2027
- Reason
- Add device or group
From the company website
Per Telefon: +49 (0)30 2350700 Fax: +49 (0)30 235070-99 Per E-Mail: [email protected]
Frequently asked questions
How many devices does PAR Medizintechnik GmbH & Co. KG have in the registry?
The registry currently lists 3 devices for PAR Medizintechnik GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list PAR Medizintechnik GmbH & Co. KG's devices?
Among its 3 most recently registered devices, PAR Medizintechnik GmbH & Co. KG has devices listed in EUDAMED (3 devices), FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PAR Medizintechnik GmbH & Co. KG's devices fall under?
Among its 3 most recently registered devices, the classes recorded for PAR Medizintechnik GmbH & Co. KG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for PAR Medizintechnik GmbH & Co. KG?
EUDAMED lists 1 certificate for PAR Medizintechnik GmbH & Co. KG (quality management system) under MDR. The most recent was issued on 1 Mar 2024.
What are the newest devices from PAR Medizintechnik GmbH & Co. KG in the registry?
The most recently registered devices listed for PAR Medizintechnik GmbH & Co. KG include TONOPORT VI, LZBD Cuff Large mit D-Ring and LZBD Cuff Medium mit D-Ring.