Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1221765

FEI Number

1221765

Entity Name

MULTI-MED, INC.

City/State/Country

Keene, NH, US

Establishment Address

26 Victoria Ct, Keene, NH 03431, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

MULTI-MED, INC. (Owner Number: 1221765)

Owner / Operator Contact Address

26 Victoria Court, --, Keene, NH 03431, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K031409

PMA Number

N/A

All Registered Proprietary Names

NDSN-PK NDSN-BU NDSP-PU NDSP-PK NDSP-BU NDSN-PU NDSP-BL NDSN-BL ISP Safety Huber Needle Infusion Set

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2018-12-17
FPD	Tube, Feeding	Gastroenterology, Urology	Class 2	876.5980	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2010-12-30
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2012-10-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-01-16
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-01-16
PTI	Non-Coring (Huber) Needle	General Hospital	Class 2	880.5570	2017-12-18
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-01-16
GBM	Catheter, Urethral	Gastroenterology, Urology	Class 2	876.5130	2008-01-16

Official Correspondent

ALAN REID

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MULTI-MED, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K221518	Np Medical	NP Medical nCompass Extension Set with Stabilizing Base	2022-11-03
K953474	Medikmark, Inc.	IV START KIT	1995-10-02
K972493	Nipro Medical Corp.	NIPRO DISPOSABLE SOLUTION INFUSION SET	1997-09-18
K982672	Baxter Healthcare Corp	COLLEAGUE PUMP SYRINGE ADAPTER SET	1998-09-04
K143446	Roche Diagnostics GmbH	Accu-Chek FlexLink Plus infusion set	2015-08-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0010-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.
Z-0012-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24
Z-0013-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set, 117" (3.0 m), with 150 mL Burette (Ball-Valve Drip Chamber) (Non-DEHP); a sterile Rx IV fluid pathway device; Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.

Similar Registrations

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3030989877	INTERNATIONAL FILTER PRODUCTS DBA IFP MEDICAL	Sun Valley, CA, US
1047843	ISOMEDIX OPERATIONS INC.	SPARTANBURG, SC, US
3002807090	Sterigenics Germany GmbH	Wiesbaden Hesse, DE
3013319212	ICU MEDICAL, INC.	Lake Forest, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1221765. Last updated year: 2026. Please use registration number 1221765 when referencing this establishment in official correspondence.