FDA.reportPublic FDA data

Aliform B.V.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30315626183031562618Aliform B.V.1N2026-01-01Oxfordlaan 55 Maastricht Limburg NL 6229 EV

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
08721325283047Aliform - Celluleaf - Surgical tool for subcutaneous blunt release of fibrous septae.+31(0)686227637info@aliformsurgical.com

Registered Device Listings#

Registration key, Listing key table
Registration keyListing key
3293821911579583

GUDID#