MedtechSourcebook

MULTI-MED, INC.

Contract manufacturer ยท Keene, NH

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2008Product codes first listed, by year (tallest: 5)2026
FDA registration
1221765 (openFDA record; or search FDA's registration database)
FEI number
1221765
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
MULTI-MED, INC. (FDA owner/operator no. 1221765)
Registered address
26 Victoria Ct, Keene, NH 03431
Contract listings
24 device listings, 5 product codes, first listed Jan 16, 2008
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
FMINeedle, Hypodermic, Single LumenClass IIGeneral hospitalContract manufacturingJan 16, 2008
FPASet, Administration, IntravascularClass IIGeneral hospitalContract manufacturingJan 16, 2008
FPDTube, FeedingClass IIGastroenterology and urologyContract manufacturingJan 16, 2008
GBMCatheter, UrethralClass IIGastroenterology and urologyContract manufacturingJan 16, 2008
KNTTubes, Gastrointestinal (And Accessories)Class IIGastroenterology and urologyContract manufacturingJan 16, 2008