Seigla Medical, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000032398 FEI 3017708755
- Devices
- 4
- 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
Catalogue
- Registry: GUDID
- Registry: GUDID
LiquID .051 LP Guide Catheter Extension Ref K243691
Regimes: CE MDR 510(k) Registry: EUDAMED510(k)GUDID- Regimes: CE MDR 510(k) Registry: EUDAMED510(k)GUDID
Company details
- EUDAMED SRN
- US-MF-000032398
- FDA FEI number
- 3017708755
- DUNS number
- 035365243
- EU VAT number
- 3747138CH
- EUDAMED status
- Active
- EUDAMED registered name
- Seigla Medical, Inc.
- Registered address
- 7688, 5th Street SE, 55313, Buffalo, United States
- Website
- www.seiglamedical.com
- [email protected]
- Phone
- 7632035428+1
- PRRC contact
- Chad Kugler
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 1 Dec 2029
Intertek Medical Notified Body AB 2862 1 certificate
- 28620207793 Active
Technical documentation EU MDR
- Issued
- 17 Mar 2025
- Expires
- 1 Dec 2029
Frequently asked questions
How many devices does Seigla Medical, Inc. have in the registry?
The registry currently lists 4 devices for Seigla Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seigla Medical, Inc.'s devices?
Among its 4 most recently registered devices, Seigla Medical, Inc. has devices listed in EUDAMED (2 devices), FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Seigla Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Seigla Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Seigla Medical, Inc.?
EUDAMED lists 1 certificate for Seigla Medical, Inc. (technical documentation) under MDR. 1 is recorded with the status issued. The most recent was issued on 2025-03-17.
What are the newest devices from Seigla Medical, Inc. in the registry?
The most recently registered devices listed for Seigla Medical, Inc. include LiquID 061 6F, LiquID 071 7F, LiquID .051 LP Guide Catheter Extension and LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension.