Ranfac Corp.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000008871 FEI 1211566
Ranfac Corp. is a medical device manufacturer based in the United States, with 281 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class IIa) as of 13 Nov 2026.
- Devices
- 281
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 266
- EUDAMED 55
- FDA 510(k) 15
- Device classes
- FDA Class II 174
- EU Class IIa 53
- FDA Class I 51
- Top EMDN categories
- Sites and related companies
- Emergo Europe B.V. authorised representative
- Identifiers
- EUDAMED SRN US-MF-000008871
- FDA FEI 1211566
- DUNS 121622872
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- Emergo Europe B.V.NL
What Ranfac Corp. makes
Ranfac Corp. manufactures medical devices including bone access cannulas, diskectomy systems, haematological concentrate system preparation kits, bone marrow biopsy needles, needle guides, bone marrow biopsy procedure kits, non-fixed blood collection needles, and rigid endoscopic cannulas.
The company's portfolio includes Class I, Class II, and Class IIa devices listed in eudamed, fda_510k, and fda_udi registries. Ranfac Corp. is based in the US.
Catalogue
Search and filter all 281 devicesShowing 1-50 of 281
Company details
- EUDAMED SRN
- US-MF-000008871
- FDA FEI number
- 1211566
- DUNS number
- 121622872
- EUDAMED status
- Active
- EUDAMED registered name
- Ranfac Corp.
- EUDAMED abbreviated name
- Ranfac Corp.
- Registered address
- 30, Doherty Avenue, 02322, Avon, United States
- Website
- ranfac.com
- info@ranfac.com
- Phone
- 15085884400
- PRRC contact
- Eric Kruez
Frequently asked questions
How many devices does RANFAC CORP. have in the registry?
The registry currently lists 281 devices for RANFAC CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list RANFAC CORP.'s devices?
Among its 50 most recently registered devices, RANFAC CORP. has devices listed in EUDAMED (1 device) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do RANFAC CORP.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for RANFAC CORP.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from RANFAC CORP. in the registry?
The most recently registered devices listed for RANFAC CORP. include CERVOS PLATELET SEPARATOR 80 KIT CER-PRP-80, HYDRACELL-ORTHO-5 11 Gauge x 6.1CM 5cc, HYDRACELL-EXT-10 11 Gauge x 6.3 CM 10cc and HYDRACELL-ORTHO-10 11 Gauge x 6.1CM 10cc.